PedAM

Pediatric Disease Annotations & Medicines


	behcet syndrome

Disease ID	357
Disease	behcet syndrome
Definition	Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well.
Synonym	adamantiades behcet disease adamantiades-behcet disease adamantiades-behcet diseases adamantiades-behcet syndrome behç beh?et's syndrome beh?et's syndrome (disorder) behcet dis behcet disease behcet diseases behcet recurrent disease behcet syndrome [disease/finding] behcet triple symptom complex behcet's behcet's disease behcet's disease (disorder) behcet's disease, nos behcet's syndrome behcet's syndrome (disorder) behcet's syndrome, nos behcets disease behcets syndrome behÃ§et disease behÃ§et diseases behÃ§et's syndrome behÃ§et's syndrome (disorder) behÃ°cet's disease complex, triple symptom complices, triple symptom disease, adamantiades-behcet disease, behÃ§et diseases, adamantiades-behcet diseases, behÃ§et et disease et syndrome et's syndrome et-adamantiades syndrome morbus behç oculobuccogenital syndrome old silk route disease silk road disease symptom complex, triple symptom complices, triple syndrome behcet's triple symptom complex triple symptom complices triple-symptom complex
Orphanet	ORPHANET:117
OMIM	OMIM:109650
DOID	DOID:13241
UMLS	C0004943
MeSH	D001528
SNOMED-CT	SNOMEDCT_US_2016_09_01:310701003
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:3) C0017661 \| iga nephropathy \| 1 C0040053 \| thrombosis \| 1 C0042384 \| vasculitis \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:27) ICAM1 \| 3383 \| CTD_human FAS \| 355 \| ORPHANET KLRC4 \| 8302 \| CTD_human;ORPHANET;GWASCAT APOA1 \| 335 \| CTD_human NOD2 \| 64127 \| ORPHANET STAT4 \| 6775 \| CTD_human;ORPHANET;GWASCAT HLA-B \| 3106 \| CTD_human;ORPHANET;GHR ITGAL \| 3683 \| CTD_human CAT \| 847 \| CTD_human APOB \| 338 \| CTD_human IL23R \| 149233 \| ORPHANET IL10 \| 3586 \| CTD_human;ORPHANET;GWASCAT UBAC2 \| 337867 \| ORPHANET ERAP1 \| 51752 \| CTD_human;GWASCAT;ORPHANET ITGB2 \| 3689 \| CTD_human IL12A-AS1 \| 101928376 \| GWASCAT;ORPHANET CCR1 \| 1230 \| CTD_human;ORPHANET SERPINE1 \| 5054 \| CTD_human TLR4 \| 7099 \| ORPHANET MEFV \| 4210 \| ORPHANET C4A \| 720 \| ORPHANET CXCL8 \| 3576 \| CTD_human IL12RB2 \| 3595 \| ORPHANET PSORS1C1 \| 170679 \| CTD_human;GWASCAT KLRC4-KLRK1 \| 100528032 \| GWASCAT IL12A \| 3592 \| ORPHANET TFCP2L1 \| 29842 \| GWASCAT
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:173) 340273 \| ABCB5 \| infer 1636 \| ACE \| infer 23205 \| ACSBG1 \| infer 56999 \| ADAMTS9 \| infer 348 \| APOE \| infer 51665 \| ASB1 \| infer 534 \| ATP6V1G2 \| infer 647076 \| BRD7P2 \| infer 56913 \| C1GALT1 \| infer 29113 \| C6orf15 \| infer 100128390 \| CALM2P1 \| infer 146849 \| CCDC42 \| infer 54535 \| CCHCR1 \| infer 1232 \| CCR3 \| infer 1234 \| CCR5 \| infer 222256 \| CDHR3 \| infer 23552 \| CDK20 \| infer 1041 \| CDSN \| infer 1051 \| CEBPB \| infer 23122 \| CLASP2 \| infer 114657 \| COX7BP1 \| infer 10815 \| CPLX1 \| infer 64478 \| CSMD1 \| infer 1493 \| CTLA4 \| infer 780 \| DDR1 \| infer 729816 \| DHFRP2 \| infer 135656 \| DPCR1 \| infer 25827 \| FBXL2 \| infer 2212 \| FCGR2A \| infer 2214 \| FCGR3A \| infer 2215 \| FCGR3B \| infer 27086 \| FOXP1 \| infer 53827 \| FXYD5 \| infer 79443 \| FYCO1 \| infer 2823 \| GPM6A \| infer 2944 \| GSTM1 \| infer 2952 \| GSTT1 \| infer 3002 \| GZMB \| infer 9421 \| HAND1 \| infer 414777 \| HCG18 \| infer 285834 \| HCG22 \| infer 352961 \| HCG26 \| infer 253018 \| HCG27 \| infer 10255 \| HCG9 \| infer 10866 \| HCP5 \| infer 3105 \| HLA-A \| infer 3106 \| HLA-B \| infer 3107 \| HLA-C \| infer 3112 \| HLA-DOB \| infer 3123 \| HLA-DRB1 \| infer 3133 \| HLA-E \| infer 3134 \| HLA-F \| infer 3135 \| HLA-G \| infer 267015 \| HLA-S \| infer 3383 \| ICAM1 \| infer 8870 \| IER3 \| infer 340198 \| IFITM4P \| infer 3439 \| IFNA1 \| infer 3455 \| IFNAR2 \| infer 3586 \| IL10 \| infer 3595 \| IL12RB2 \| infer 3606 \| IL18 \| infer 3552 \| IL1A \| infer 3553 \| IL1B \| infer 7850 \| IL1R2 \| infer 3557 \| IL1RN \| infer 116379 \| IL22RA2 \| infer 149233 \| IL23R \| infer 286676 \| ILDR1 \| infer 91464 \| ISX \| infer 3720 \| JARID2 \| infer 3802 \| KIR2DL1 \| infer 3803 \| KIR2DL2 \| infer 3804 \| KIR2DL3 \| infer 3805 \| KIR2DL4 \| infer 57292 \| KIR2DL5A \| infer 3806 \| KIR2DS1 \| infer 100132285 \| KIR2DS2 \| infer 3808 \| KIR2DS3 \| infer 3809 \| KIR2DS4 \| infer 3810 \| KIR2DS5 \| infer 3811 \| KIR3DL1 \| infer 3812 \| KIR3DL2 \| infer 115653 \| KIR3DL3 \| infer 3813 \| KIR3DS1 \| infer 3821 \| KLRC1 \| infer 3822 \| KLRC2 \| infer 283455 \| KSR2 \| infer 4049 \| LTA \| infer 54585 \| LZTFL1 \| infer 401250 \| MCCD1 \| infer 23101 \| MCF2L2 \| infer 55784 \| MCTP2 \| infer 9656 \| MDC1 \| infer 100507436 \| MICA \| infer 4277 \| MICB \| infer 100129192 \| MICC \| infer 4279 \| MICD \| infer 4280 \| MICE \| infer 4318 \| MMP9 \| infer 4340 \| MOG \| infer 4353 \| MPO \| infer 394263 \| MUC21 \| infer 10 \| NAT2 \| infer 259197 \| NCR3 \| infer 4792 \| NFKBIA \| infer 4795 \| NFKBIL1 \| infer 286053 \| NSMCE2 \| infer 57157 \| PHTF2 \| infer 5460 \| POU5F1 \| infer 5491 \| PPIAP9 \| infer 5514 \| PPP1R10 \| infer 170679 \| PSORS1C1 \| infer 170680 \| PSORS1C2 \| infer 100130889 \| PSORS1C3 \| infer 326627 \| RANBP20P \| infer 80352 \| RNF39 \| infer 6148 \| RPL23AP1 \| infer 116935 \| RPL3P2 \| infer 729123 \| RPL7P21 \| infer 728823 \| RPS26P53 \| infer 100270859 \| RPS2P19 \| infer 23429 \| RYBP \| infer 223117 \| SEMA3D \| infer 389376 \| SFTA2 \| infer 6556 \| SLC11A1 \| infer 112574 \| SNX18 \| infer 6775 \| STAT4 \| infer 285829 \| SUMO2P1 \| infer 387082 \| SUMO4 \| infer 57057 \| TBX20 \| infer 6941 \| TCF19 \| infer 7097 \| TLR2 \| infer 7099 \| TLR4 \| infer 54106 \| TLR9 \| infer 387890 \| TMEM233 \| infer 7124 \| TNF \| infer 7726 \| TRIM26 \| infer 11074 \| TRIM31 \| infer 10537 \| UBD \| infer 134111 \| UBE2QL1 \| infer 7342 \| UBP1 \| infer 387117 \| UBQLN1P1 \| infer 57176 \| VARS2 \| infer 387122 \| WASF5P \| infer 57705 \| WDFY4 \| infer 25937 \| WWTR1 \| infer 2829 \| XCR1 \| infer 346171 \| ZFP57 \| infer 54504 \| CPVL \| infer 337867 \| UBAC2 \| infer 84959 \| UBASH3B \| infer 6347 \| CCL2 \| infer 940 \| CD28 \| infer 1543 \| CYP1A1 \| infer 1557 \| CYP2C19 \| infer 1559 \| CYP2C9 \| infer 2147 \| F2 \| infer 2153 \| F5 \| infer 2220 \| FCN2 \| infer 3673 \| ITGA2 \| infer 3952 \| LEP \| infer 4153 \| MBL2 \| infer 4210 \| MEFV \| infer 4598 \| MVK \| infer 114548 \| NLRP3 \| infer 4846 \| NOS3 \| infer 9051 \| PSTPIP1 \| infer 6648 \| SOD2 \| infer 6649 \| SOD3 \| infer 6890 \| TAP1 \| infer 6891 \| TAP2 \| infer 7422 \| VEGFA \| infer
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:298) 7132 \| TNFRSF1A \| DISEASES 30009 \| TBX21 \| DISEASES 1361 \| CPB2 \| DISEASES 2191 \| FAP \| DISEASES 350 \| APOH \| DISEASES 7049 \| TGFBR3 \| DISEASES 4282 \| MIF \| DISEASES 3957 \| LGALS2 \| DISEASES 10544 \| PROCR \| DISEASES 51311 \| TLR8 \| DISEASES 4210 \| MEFV \| DISEASES 51285 \| RASL12 \| DISEASES 5327 \| PLAT \| DISEASES 8797 \| TNFRSF10A \| DISEASES 56729 \| RETN \| DISEASES 973 \| CD79A \| DISEASES 5444 \| PON1 \| DISEASES 10392 \| NOD1 \| DISEASES 5054 \| SERPINE1 \| DISEASES 26157 \| GIMAP2 \| DISEASES 5949 \| RBP3 \| DISEASES 6348 \| CCL3 \| DISEASES 4353 \| MPO \| DISEASES 6347 \| CCL2 \| DISEASES 6372 \| CXCL6 \| DISEASES 4790 \| NFKB1 \| DISEASES 3558 \| IL2 \| DISEASES 969 \| CD69 \| DISEASES 4598 \| MVK \| DISEASES 51561 \| IL23A \| DISEASES 3458 \| IFNG \| DISEASES 55907 \| CMAS \| DISEASES 3111 \| HLA-DOA \| DISEASES 3565 \| IL4 \| DISEASES 7035 \| TFPI \| DISEASES 6556 \| SLC11A1 \| DISEASES 338 \| APOB \| DISEASES 3554 \| IL1R1 \| DISEASES 5657 \| PRTN3 \| DISEASES 116444 \| GRIN3B \| DISEASES 2023 \| ENO1 \| DISEASES 6402 \| SELL \| DISEASES 7128 \| TNFAIP3 \| DISEASES 6431 \| SRSF6 \| DISEASES 1088 \| CEACAM8 \| DISEASES 80352 \| RNF39 \| DISEASES 54210 \| TREM1 \| DISEASES 2069 \| EREG \| DISEASES 30833 \| NT5C \| DISEASES 10893 \| MMP24 \| DISEASES 10870 \| HCST \| DISEASES 1236 \| CCR7 \| DISEASES 4708 \| NDUFB2 \| DISEASES 58509 \| CACTIN \| DISEASES 968 \| CD68 \| DISEASES 11026 \| LILRA3 \| DISEASES 5157 \| PDGFRL \| DISEASES 4277 \| MICB \| DISEASES 1401 \| CRP \| DISEASES 55303 \| GIMAP4 \| DISEASES 4064 \| CD180 \| DISEASES 80210 \| ARMC9 \| DISEASES 55270 \| NUDT15 \| DISEASES 3569 \| IL6 \| DISEASES 3557 \| IL1RN \| DISEASES 27348 \| TOR1B \| DISEASES 6366 \| CCL21 \| DISEASES 170679 \| PSORS1C1 \| DISEASES 3134 \| HLA-F \| DISEASES 7097 \| TLR2 \| DISEASES 1559 \| CYP2C9 \| DISEASES 4069 \| LYZ \| DISEASES 7450 \| VWF \| DISEASES 7188 \| TRAF5 \| DISEASES 3595 \| IL12RB2 \| DISEASES 9135 \| RABEP1 \| DISEASES 51816 \| CECR1 \| DISEASES 64377 \| CHST8 \| DISEASES 671 \| BPI \| DISEASES 5588 \| PRKCQ \| DISEASES 27178 \| IL37 \| DISEASES 3552 \| IL1A \| DISEASES 3553 \| IL1B \| DISEASES 735 \| C9 \| DISEASES 55717 \| WDR11 \| DISEASES 1991 \| ELANE \| DISEASES 6403 \| SELP \| DISEASES 5775 \| PTPN4 \| DISEASES 4811 \| NID1 \| DISEASES 941 \| CD80 \| DISEASES 8807 \| IL18RAP \| DISEASES 7294 \| TXK \| DISEASES 1356 \| CP \| DISEASES 6774 \| STAT3 \| DISEASES 3383 \| ICAM1 \| DISEASES 54504 \| CPVL \| DISEASES 939 \| CD27 \| DISEASES 3687 \| ITGAX \| DISEASES 3394 \| IRF8 \| DISEASES 6687 \| SPG7 \| DISEASES 28987 \| NOB1 \| DISEASES 5141 \| PDE4A \| DISEASES 2212 \| FCGR2A \| DISEASES 3001 \| GZMA \| DISEASES 3439 \| IFNA1 \| DISEASES 133 \| ADM \| DISEASES 726 \| CAPN5 \| DISEASES 3606 \| IL18 \| DISEASES 5458 \| POU4F2 \| DISEASES 83734 \| ATG10 \| DISEASES 55079 \| FEZF2 \| DISEASES 84959 \| UBASH3B \| DISEASES 1636 \| ACE \| DISEASES 115650 \| TNFRSF13C \| DISEASES 1234 \| CCR5 \| DISEASES 6352 \| CCL5 \| DISEASES 7412 \| VCAM1 \| DISEASES 2215 \| FCGR3B \| DISEASES 3577 \| CXCR1 \| DISEASES 50852 \| TRAT1 \| DISEASES 213 \| ALB \| DISEASES 1230 \| CCR1 \| DISEASES 3600 \| IL15 \| DISEASES 51752 \| ERAP1 \| DISEASES 7098 \| TLR3 \| DISEASES 1437 \| CSF2 \| DISEASES 1669 \| DEFA4 \| DISEASES 4846 \| NOS3 \| DISEASES 9150 \| CTDP1 \| DISEASES 26253 \| CLEC4E \| DISEASES 64127 \| NOD2 \| DISEASES 170575 \| GIMAP1 \| DISEASES 3308 \| HSPA4 \| DISEASES 3688 \| ITGB1 \| DISEASES 1673 \| DEFB4A \| DISEASES 1493 \| CTLA4 \| DISEASES 3596 \| IL13 \| DISEASES 10815 \| CPLX1 \| DISEASES 3627 \| CXCL10 \| DISEASES 10963 \| STIP1 \| DISEASES 56246 \| MRAP \| DISEASES 6373 \| CXCL11 \| DISEASES 2147 \| F2 \| DISEASES 5340 \| PLG \| DISEASES 8302 \| KLRC4 \| DISEASES 84868 \| HAVCR2 \| DISEASES 55075 \| UACA \| DISEASES 23075 \| SWAP70 \| DISEASES 57381 \| RHOJ \| DISEASES 144811 \| LACC1 \| DISEASES 4684 \| NCAM1 \| DISEASES 387082 \| SUMO4 \| DISEASES 3579 \| CXCR2 \| DISEASES 80381 \| CD276 \| DISEASES 140596 \| DEFB104A \| DISEASES 414325 \| DEFB103A \| DISEASES 149233 \| IL23R \| DISEASES 5345 \| SERPINF2 \| DISEASES 503618 \| DEFB104B \| DISEASES 26061 \| HACL1 \| DISEASES 2 \| A2M \| DISEASES 55894 \| DEFB103B \| DISEASES 6097 \| RORC \| DISEASES 55258 \| THNSL2 \| DISEASES 6401 \| SELE \| DISEASES 2621 \| GAS6 \| DISEASES 942 \| CD86 \| DISEASES 285525 \| YIPF7 \| DISEASES 8690 \| JRKL \| DISEASES 151888 \| BTLA \| DISEASES 503841 \| DEFB106B \| DISEASES 245909 \| DEFB106A \| DISEASES 3802 \| KIR2DL1 \| DISEASES 114548 \| NLRP3 \| DISEASES 112744 \| IL17F \| DISEASES 55146 \| ZDHHC4 \| DISEASES 3824 \| KLRD1 \| DISEASES 445329 \| SULT1A4 \| DISEASES 3117 \| HLA-DQA1 \| DISEASES 3805 \| KIR2DL4 \| DISEASES 3329 \| HSPD1 \| DISEASES 5493 \| PPL \| DISEASES 5810 \| RAD1 \| DISEASES 1447 \| CSN2 \| DISEASES 3804 \| KIR2DL3 \| DISEASES 3716 \| JAK1 \| DISEASES 3198 \| HOXA1 \| DISEASES 6818 \| SULT1A3 \| DISEASES 545 \| ATR \| DISEASES 3605 \| IL17A \| DISEASES 387837 \| CLEC12B \| DISEASES 3767 \| KCNJ11 \| DISEASES 2109 \| ETFB \| DISEASES 3181 \| HNRNPA2B1 \| DISEASES 160364 \| CLEC12A \| DISEASES 355 \| FAS \| DISEASES 5265 \| SERPINA1 \| DISEASES 3683 \| ITGAL \| DISEASES 5350 \| PLN \| DISEASES 6775 \| STAT4 \| DISEASES 3821 \| KLRC1 \| DISEASES 10814 \| CPLX2 \| DISEASES 26191 \| PTPN22 \| DISEASES 3123 \| HLA-DRB1 \| DISEASES 2157 \| F8 \| DISEASES 3135 \| HLA-G \| DISEASES 54106 \| TLR9 \| DISEASES 9267 \| CYTH1 \| DISEASES 4283 \| CXCL9 \| DISEASES 7096 \| TLR1 \| DISEASES 6993 \| DYNLT1 \| DISEASES 462 \| SERPINC1 \| DISEASES 2214 \| FCGR3A \| DISEASES 115352 \| FCRL3 \| DISEASES 8517 \| IKBKG \| DISEASES 8804 \| CREG1 \| DISEASES 959 \| CD40LG \| DISEASES 1757 \| SARDH \| DISEASES 7422 \| VEGFA \| DISEASES 958 \| CD40 \| DISEASES 4318 \| MMP9 \| DISEASES 100 \| ADA \| DISEASES 1025 \| CDK9 \| DISEASES 139599 \| MAGEE2 \| DISEASES 23787 \| MTCH1 \| DISEASES 2833 \| CXCR3 \| DISEASES 4153 \| MBL2 \| DISEASES 7099 \| TLR4 \| DISEASES 3339 \| HSPG2 \| DISEASES 10673 \| TNFSF13B \| DISEASES 50943 \| FOXP3 \| DISEASES 100507436 \| MICA \| DISEASES 3107 \| HLA-C \| DISEASES 6941 \| TCF19 \| DISEASES 7133 \| TNFRSF1B \| DISEASES 1041 \| CDSN \| DISEASES 4524 \| MTHFR \| DISEASES 2794 \| GNL1 \| DISEASES 3133 \| HLA-E \| DISEASES 56658 \| TRIM39 \| DISEASES 11074 \| TRIM31 \| DISEASES 3105 \| HLA-A \| DISEASES 7056 \| THBD \| DISEASES 23130 \| ATG2A \| DISEASES 84210 \| ANKRD20A1 \| DISEASES 1906 \| EDN1 \| DISEASES 3559 \| IL2RA \| DISEASES 54790 \| TET2 \| DISEASES 3440 \| IFNA2 \| DISEASES 3456 \| IFNB1 \| DISEASES 51284 \| TLR7 \| DISEASES 90865 \| IL33 \| DISEASES 3822 \| KLRC2 \| DISEASES 3823 \| KLRC3 \| DISEASES 10333 \| TLR6 \| DISEASES 83650 \| SLC35G5 \| DISEASES 1667 \| DEFA1 \| DISEASES 728358 \| DEFA1B \| DISEASES 402682 \| UFSP1 \| DISEASES 3811 \| KIR3DL1 \| DISEASES 2524 \| FUT2 \| DISEASES 114609 \| TIRAP \| DISEASES 3895 \| KTN1 \| DISEASES 2919 \| CXCL1 \| DISEASES 3652 \| IPP \| DISEASES 80380 \| PDCD1LG2 \| DISEASES 3119 \| HLA-DQB1 \| DISEASES 3803 \| KIR2DL2 \| DISEASES 337867 \| UBAC2 \| DISEASES 23308 \| ICOSLG \| DISEASES 6295 \| SAG \| DISEASES 55660 \| PRPF40A \| DISEASES 3120 \| HLA-DQB2 \| DISEASES 11277 \| TREX1 \| DISEASES 121512 \| FGD4 \| DISEASES 55683 \| KANSL3 \| DISEASES 7124 \| TNF \| DISEASES 3106 \| HLA-B \| DISEASES 64167 \| ERAP2 \| DISEASES 3594 \| IL12RB1 \| DISEASES 4049 \| LTA \| DISEASES 254827 \| NAALADL2 \| DISEASES 3115 \| HLA-DPB1 \| DISEASES 389549 \| FEZF1 \| DISEASES 3586 \| IL10 \| DISEASES 133396 \| IL31RA \| DISEASES 51428 \| DDX41 \| DISEASES 284 \| ANGPT1 \| DISEASES 22999 \| RIMS1 \| DISEASES 930 \| CD19 \| DISEASES 1232 \| CCR3 \| DISEASES 3684 \| ITGAM \| DISEASES 9051 \| PSTPIP1 \| DISEASES 567 \| B2M \| DISEASES 820 \| CAMP \| DISEASES 285830 \| HLA-F-AS1 \| DISEASES 101928376 \| IL12A-AS1 \| DISEASES 102659353 \| THRIL \| DISEASES
Locus	(Waiting for update.)

Disease ID	357
Disease	behcet syndrome
Integrated Phenotype	HPO \| Name(Total Integrated Phenotypes:11) HP:0000155 \| Oral ulcer HP:0000737 \| Irritability HP:0001094 \| Iridocyclitis HP:0003249 \| Genital ulcers HP:0002229 \| Alopecia areata HP:0001369 \| Arthritis HP:0012424 \| Chorioretinitis HP:0002638 \| Superficial thrombophlebitis HP:0000031 \| Epididymitis HP:0001101 \| Iritis HP:0010783 \| Erythema
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:2) HP:0012089 \| Arteritis \| 1 HP:0002633 \| Vasculitis \| 1

Disease ID	357
Disease	behcet syndrome
Manually Symptom	(Waiting for update.)
Text Mined Symptom	(Waiting for update.)

Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)

All Snps(Total Genotypes:243)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs10049211	20622878	23429	RYBP	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	3	72465525	T	C
rs10050860	26097239	1230	CCR1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120814326	2015	ERAP1	5	96786506	C	T
rs10050860	26097239	101928376	IL12A-AS1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120271442	2015	ERAP1	5	96786506	C	T
rs10204525	22039410	80380	PDCD1LG2	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1	2	241850169	C	T
rs10204525	22039410	5133	PDCD1	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1	2	241850169	C	T
rs10204525	22039410	29126	CD274	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1	2	241850169	C	T
rs10456378	20622878	7726	TRIM26	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30238409	G	A
rs1045642	24898446	5243	ABCB1	umls:C0004943	BeFree	MDR1 C3435T polymorphism associated with the development of clinical features in Behçet's disease in Iranian Azeri Turkish patients.	0.000814326	2015	ABCB1	7	87509329	A	T,G
rs10460943	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	3	71623155	C	T
rs10486156	20622878	56913	C1GALT1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	7	7309002	C	T
rs10510749	20622878	2829	XCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LOC105377067	3	46138924	C	T
rs10510933	20622878	56999	ADAMTS9	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LOC105377127	3	65162946	G	A
rs10513355	20622878	25937	WWTR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	WWTR1	3	149533572	A	G
rs1062470	20622878	1041	CDSN	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CDSN;PSORS1C1	6	31116658	G	A
rs1062470	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	CDSN;PSORS1C1	6	31116658	G	A
rs10868677	20622878	23552	CDK20	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	9	87996957	C	T
rs10940434	20622878	112574	SNX18	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	5	54879078	T	C
rs10947058	20622878	7726	TRIM26	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	TRIM26	6	30208345	C	T
rs11072744	20622878	23205	ACSBG1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ACSBG1	15	78218477	G	T
rs11128275	20622878	23429	RYBP	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	3	72466809	G	A
rs111614996	20622878	3107	HLA-C	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.010282454	2010	NA	NA	NA	NA	NA
rs113112186	20622878	5460	POU5F1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	NA	NA	NA	NA
rs113198053	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	NA	NA	NA	NA
rs113481038	20622878	54535	CCHCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	NA	NA	NA	NA
rs11466023	25318808	4210	MEFV	umls:C0004943	BeFree	Mediterranean fever (MEFV) variant P369S/R408Q in a patient with entero-Behçet's disease who successfully responded to treatment with colchicine.	0.14225569	2015	MEFV	16	3249586	G	T,A
rs11466024	25318808	4210	MEFV	umls:C0004943	BeFree	Mediterranean fever (MEFV) variant P369S/R408Q in a patient with entero-Behçet's disease who successfully responded to treatment with colchicine.	0.14225569	2015	MEFV	16	3249468	C	T
rs116799036	25889189	3106	HLA-B	umls:C0004943	BeFree	We found that the HLA-B51 allele and the rs76546355/rs116799036 MHC SNP are independent genetic risk factors for BD in Iranian, and that positivity for the rs76546355/rs116799036 risk allele, but not for B51, does correlate with specific demographic characteristics or clinical manifestations in BD patients.	0.346098146	2015	NA	NA	NA	NA	NA
rs116799036	23396137	100507436	MICA	umls:C0004943	BeFree	Our data suggest that the robust HLA-B*51 association in Behçet's disease is explained by a variant located between the HLA-B and MICA genes (rs116799036: odds ratio (OR) = 3.88, P = 9.42 × 10(-50)).	0.013811198	2013	NA	NA	NA	NA	NA
rs116799036	23396137	3106	HLA-B	umls:C0004943	BeFree	Our data suggest that the robust HLA-B*51 association in Behçet's disease is explained by a variant located between the HLA-B and MICA genes (rs116799036: odds ratio (OR) = 3.88, P = 9.42 × 10(-50)).	0.346098146	2013	NA	NA	NA	NA	NA
rs11718322	20622878	286676	ILDR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ILDR1	3	121991239	G	A
rs11720121	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71546107	T	C
rs11720523	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71496019	C	A
rs11962776	20622878	3720	JARID2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	JARID2	6	15259922	C	A
rs11967883	20622878	54535	CCHCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CCHCR1	6	31144577	C	T
rs12487660	20622878	23122	CLASP2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CLASP2	3	33551080	T	G
rs12639224	20622878	54585	LZTFL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LZTFL1	3	45874730	C	T
rs1264298	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30916659	A	G
rs1264301	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30915004	G	T,A
rs1264302	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30914857	C	T
rs1264303	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30914736	A	G
rs1264327	20622878	780	DDR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDR1	6	30882805	G	A
rs1264331	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDR1	6	30879053	G	T
rs1264332	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30877786	G	C
rs1264333	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30876537	T	C
rs1264362	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30808813	C	G
rs1264459	20622878	3133	HLA-E	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.013625632	2010	HLA-E	6	30488143	G	A
rs1265062	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31110228	C	T
rs13154629	26097239	101928376	IL12A-AS1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120271442	2015	ERAP1	5	96786754	C	T
rs13154629	26097239	1230	CCR1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120814326	2015	ERAP1	5	96786754	C	T
rs1357540	20622878	7342	UBP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	UBP1	3	33438490	T	C
rs1362126	20622878	3134	HLA-F	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002638474	2010	HLA-F	6	29723242	G	A
rs1495714	20622878	2823	GPM6A	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	GPM6A	4	175916638	C	A
rs1495965	20622878	149233	IL23R	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.130358398	2010	NA	1	67287825	C	T
rs1495965	20622879	149233	IL23R	umls:C0004943	GAD	[Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci.]	0.130358398	2010	NA	1	67287825	C	T
rs1495966	20622878	149233	IL23R	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.130358398	2010	NA	1	67287670	T	C
rs1518111	20622878	3586	IL10	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.375906788	2010	IL10	1	206771300	T	C
rs1518111	20622878	3586	IL10	umls:C0004943	GWASCAT	Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.	0.375906788	2010	IL10	1	206771300	T	C
rs17006292	23001997	29842	TFCP2L1	umls:C0004943	GWASCAT	Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.	0.12	2012	TFCP2L1	2	121261187	C	A
rs17190071	20622878	394263	MUC21	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	MUC22	6	31031926	G	A
rs17190526	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	C6orf15;PSORS1C1	6	31114304	G	A
rs17190526	20622878	29113	C6orf15	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	C6orf15;PSORS1C1	6	31114304	G	A
rs17196989	20622878	54535	CCHCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CCHCR1	6	31145926	A	G
rs17302884	20622878	493913	PAPPA-AS1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	9	116409768	A	G
rs17482078	23291587	51752	ERAP1	umls:C0004943	GWASCAT	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	0.242171535	2013	ERAP1;LOC102724748	5	96783162	C	G,T
rs17482078	23291587	102724748	LOC102724748	umls:C0004943	GWASCAT	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	0.12	2013	ERAP1;LOC102724748	5	96783162	C	G,T
rs17810546	25799145	101928376	IL12A-AS1	umls:C0004943	GWASCAT	Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease.	0.120271442	2015	IL12A-AS1	3	159947262	A	G
rs17810546	26097239	101928376	IL12A-AS1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120271442	2015	IL12A-AS1	3	159947262	A	G
rs17810546	26097239	1230	CCR1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120814326	2015	IL12A-AS1	3	159947262	A	G
rs17810546	23291587	101928376	IL12A-AS1	umls:C0004943	GWASCAT	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	0.120271442	2013	IL12A-AS1	3	159947262	A	G
rs1799983	16463158	4846	NOS3	umls:C0004943	BeFree	Lack of evidence for association between endothelial nitric oxide synthase gene polymorphism (glu298asp) with Behçet's disease in the Turkish population.	0.025089661	2006	NOS3	7	150999023	T	G
rs1799983	17067432	4846	NOS3	umls:C0004943	BeFree	Endothelial nitric oxide synthase gene Glu298Asp polymorphism is associated with Behçet's disease.	0.025089661	2006	NOS3	7	150999023	T	G
rs1800871	20622879	3586	IL10	umls:C0004943	GWASCAT	Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.	0.375906788	2010	IL10	1	206773289	A	G
rs1800871	20622879	3586	IL10	umls:C0004943	GAD	[Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci.]	0.375906788	2010	IL10	1	206773289	A	G
rs1807844	20622878	7342	UBP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	UBP1	3	33431445	T	C
rs1882191	20622878	196446	MYRFL	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	12	69991543	C	T
rs1970000	22039410	29126	CD274	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	CD274	9	5465036	C	A
rs1970000	22039410	80380	PDCD1LG2	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	CD274	9	5465036	C	A
rs1970000	22039410	5133	PDCD1	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	CD274	9	5465036	C	A
rs1971773	20622878	146849	CCDC42	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CCDC42	17	8729992	C	T
rs2009658	20622878	4049	LTA	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.007915422	2010	LTA;LOC100287329	6	31570467	C	G
rs2046006	20622878	55784	MCTP2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	15	94694732	C	A
rs2061634	19442274	100499483	CCDC180	umls:C0004943	BeFree	Among the associated SNPs, the Behçet's disease-risk allele in rs2061634 leads to substitution of serine to cysteine at amino acid position 995 (S995C) in the KIAA1529 protein.	0.000271442	2009	LOC100499484-C9ORF174;CCDC180	9	97343500	C	G
rs2071593	20622878	4795	NFKBIL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ATP6V1G2;NFKBIL1;ATP6V1G2-DDX39B	6	31545022	G	A
rs2071593	20622878	534	ATP6V1G2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ATP6V1G2;NFKBIL1;ATP6V1G2-DDX39B	6	31545022	G	A
rs2071653	20622878	4340	MOG	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	MOG	6	29668151	T	C
rs2074478	20622878	170680	PSORS1C2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	PSORS1C1;PSORS1C2	6	31137856	C	T
rs2074478	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	PSORS1C1;PSORS1C2	6	31137856	C	T
rs2074506	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30922706	G	T
rs2121037	20622878	144811	LACC1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	13	43897181	C	T
rs2133660	20622878	79443	FYCO1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FYCO1	3	45990465	C	T
rs2187961	20622878	91464	ISX	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LINC01399	22	35185406	G	A
rs2199724	20622878	55784	MCTP2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	15	94691904	G	T
rs2227981	22039410	29126	CD274	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1;LOC105373977	2	241851121	A	G,C
rs2227981	22039410	80380	PDCD1LG2	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1;LOC105373977	2	241851121	A	G,C
rs2227981	22039410	5133	PDCD1	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1;LOC105373977	2	241851121	A	G,C
rs2229094	20622878	4049	LTA	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.007915422	2010	LTA;LOC100287329	6	31572779	T	C
rs2230365	20622878	4795	NFKBIL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NFKBIL1;LOC100287329	6	31557671	C	T
rs2233965	20622878	29113	C6orf15	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	C6orf15;PSORS1C1	6	31113122	T	G
rs2233965	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	C6orf15;PSORS1C1	6	31113122	T	G
rs2233967	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	C6orf15;PSORS1C1	6	31113051	C	G
rs2233967	20622878	29113	C6orf15	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	C6orf15;PSORS1C1	6	31113051	C	G
rs2239709	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;ATP6V1G2-DDX39B	6	31539670	C	T
rs2240804	20622878	135656	DPCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DPCR1;LOC102723346	6	30953113	G	A
rs2250264	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30853410	G	A
rs2251824	20622878	534	ATP6V1G2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ATP6V1G2;DDX39B;ATP6V1G2-DDX39B	6	31544080	G	A
rs2251824	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ATP6V1G2;DDX39B;ATP6V1G2-DDX39B	6	31544080	G	A
rs2251830	20622878	394263	MUC21	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31049201	C	A
rs2255798	20622878	4795	NFKBIL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NFKBIL1;LOC100287329	6	31553525	G	C
rs2285515	20622878	53827	FXYD5	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FXYD5	19	35169547	T	C
rs228648	23333481	10911	UTS2	umls:C0004943	BeFree	Thr21Met (T21M) but not Ser89Asn (S89N) polymorphisms of the urotensin-II (UTS-II) gene are associated with Behcet's disease (BD).	0.000271442	2012	UTS2	1	7853370	G	A
rs2291897	20622878	25827	FBXL2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FBXL2	3	33377930	C	T
rs231775	24991555	1493	CTLA4	umls:C0004943	BeFree	The role of CTLA-4 exon-1 49 A/G polymorphism and soluble CTLA-4 protein level in egyptian patients with Behçet's disease.	0.019012201	2014	CTLA4	2	203867991	A	G,T
rs231775	16045690	1493	CTLA4	umls:C0004943	BeFree	CTLA-4 gene 49A/G polymorphism in Turkish patients with Behçet's disease.	0.019012201	2005	CTLA4	2	203867991	A	G,T
rs231775	18498289	1493	CTLA4	umls:C0004943	BeFree	We analysed the SNPs -318C/T and 49A/G in CTLA-4 in patients with Behcet's disease (BD), patients with intermediate uveitis and appropriate controls.	0.019012201	2008	CTLA4	2	203867991	A	G,T
rs2394423	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31064265	G	A
rs2508011	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31103281	A	C
rs2516393	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;ATP6V1G2-DDX39B	6	31538967	A	C
rs2517403	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31099232	T	C
rs2517467	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30921483	G	A
rs2523500	20622878	4795	NFKBIL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NFKBIL1;LOC100287329	6	31550577	G	A
rs2523503	20622878	534	ATP6V1G2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ATP6V1G2;NFKBIL1;ATP6V1G2-DDX39B	6	31545782	C	A
rs2523503	20622878	4795	NFKBIL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	ATP6V1G2;NFKBIL1;ATP6V1G2-DDX39B	6	31545782	C	A
rs2523864	20622878	394263	MUC21	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31050769	C	T
rs2532929	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30929997	A	G
rs2532934	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30926982	G	A
rs2532938	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30926054	G	A
rs2535327	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30859127	T	C
rs2535331	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LOC105375014	6	30848493	G	A
rs2617170	23291587	100528032	KLRC4-KLRK1	umls:C0004943	GWASCAT	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	0.12	2013	KLRC4;KLRC4-KLRK1	12	10408358	T	C
rs2617170	26097239	1230	CCR1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120814326	2015	KLRC4;KLRC4-KLRK1	12	10408358	T	C
rs2617170	26097239	101928376	IL12A-AS1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120271442	2015	KLRC4;KLRC4-KLRK1	12	10408358	T	C
rs2617170	23291587	8302	KLRC4	umls:C0004943	GWASCAT	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	0.24	2013	KLRC4;KLRC4-KLRK1	12	10408358	T	C
rs2709748	20622878	340273	ABCB5	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	7	20780150	G	A
rs28362332	20622878	100130889	PSORS1C3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31194377	G	A
rs28362343	20622878	100130889	PSORS1C3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	HCG27	6	31197750	G	A
rs2844480	20622878	259197	NCR3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31597044	C	T
rs2844635	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31107704	A	G
rs2844652	20622878	389376	SFTA2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	SFTA2	6	30930910	C	T
rs2844654	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30870911	T	G
rs2844680	20622878	135656	DPCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30978719	T	G
rs2844697	20622878	135656	DPCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30964532	C	T
rs2857106	20622878	3112	HLA-DOB	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	32819793	T	C
rs2857281	20622878	57157	PHTF2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	MICA	6	31406485	A	C
rs3024490	20622878	3586	IL10	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.375906788	2010	IL10	1	206771966	A	C
rs3025652	20622878	10537	UBD	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	29571988	G	A
rs3093948	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;ATP6V1G2-DDX39B	6	31533636	A	G
rs3093976	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;ATP6V1G2-DDX39B	6	31535084	A	G
rs3093978	20622878	401250	MCCD1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;MCCD1;ATP6V1G2-DDX39B	6	31530720	C	A
rs3093978	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;MCCD1;ATP6V1G2-DDX39B	6	31530720	C	A
rs3094065	20622878	414777	HCG18	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	HCG18;HCG17	6	30314555	T	C
rs3094654	20622878	3135	HLA-G	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.007729856	2010	NA	6	29872039	T	C
rs3095089	20622878	135656	DPCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30966017	G	T
rs3130057	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;SNORD117;ATP6V1G2-DDX39B	6	31536810	G	T
rs3130058	20622878	7919	DDX39B	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	DDX39B;SNORD117;ATP6V1G2-DDX39B	6	31538110	T	C
rs3130467	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31219298	C	T
rs3130473	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31231431	C	T
rs3130931	20622878	5460	POU5F1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	POU5F1	6	31167111	T	C
rs3131643	20622878	352961	HCG26	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31475005	G	A
rs3131863	20622878	346171	ZFP57	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	29705706	G	A
rs3132726	20622878	3135	HLA-G	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.007729856	2010	LOC105375010	6	29855829	A	G
rs3135050	20622878	4340	MOG	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	MOG	6	29660660	T	C
rs34682678	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30792862	A	C
rs3764147	20622878	144811	LACC1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LACC1	13	43883789	A	G
rs3778638	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	PSORS1C1	6	31124347	G	A
rs3849150	20622878	57705	WDFY4	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	WDFY4;LRRC18	10	48901178	C	T
rs397507444	23827456	4524	MTHFR	umls:C0004943	BeFree	Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet's disease.	0.016102285	2013	MTHFR	1	11794407	T	G
rs4084090	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31251058	A	G
rs4446605	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31205319	A	G
rs4690647	20622878	2823	GPM6A	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	GPM6A;LOC105377553	4	175951769	G	A
rs4711209	20622878	80352	RNF39	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002638474	2010	NA	6	30079626	G	A
rs4851526	20622878	7850	IL1R2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	IL1R2	2	102001908	A	G
rs4865879	20622878	112574	SNX18	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	5	54864517	C	T
rs4896243	20622878	116379	IL22RA2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	137193653	C	T
rs4900016	20622878	90141	EFCAB11	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	EFCAB11	14	89839316	A	G
rs4947244	20622878	10255	HCG9	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	29986587	C	G
rs4947296	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31090401	T	C
rs4959053	23001997	170679	PSORS1C1	umls:C0004943	GWASCAT	Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.	0.242367032	2012	PSORS1C1	6	31131800	G	A
rs5025708	20622878	10255	HCG9	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	29987422	G	T
rs5498	19906207	3383	ICAM1	umls:C0004943	BeFree	Intercellular adhesion molecule 1 K469E gene polymorphism is associated with presence of skin lesions in Tunisian Behçet's disease patients.	0.133821129	2010	ICAM1;ICAM4;LOC105372272	19	10285007	A	G
rs563624	20622878	134111	UBE2QL1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	5	6521724	A	C
rs5743708	19693643	7097	TLR2	umls:C0004943	BeFree	No association of the TLR2 gene Arg753Gln polymorphism with rheumatic heart disease and Behçet's disease.	0.008729747	2009	TLR2	4	153705165	G	A
rs5743708	16901312	7097	TLR2	umls:C0004943	BeFree	Toll-like receptor 2 Arg753Gln gene polymorphism in Turkish patients with Behçet's disease.	0.008729747	2006	TLR2	4	153705165	G	A
rs6549392	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71489545	G	T
rs6549400	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71557315	T	C,G
rs6779258	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71500488	T	C
rs6904029	20622878	10255	HCG9	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	HCG9	6	29975290	G	A
rs6917517	20622878	170679	PSORS1C1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.242367032	2010	PSORS1C1	6	31114584	C	T
rs6967330	20622878	222256	CDHR3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CDHR3	7	106018005	G	A
rs6986423	20622878	64478	CSMD1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CSMD1	8	4776893	G	T
rs7004739	20622878	286053	NSMCE2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NSMCE2	8	125316141	G	A
rs7295696	20622878	283455	KSR2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	12	117993522	T	C
rs7310266	20622878	387890	TMEM233	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LOC105370027	12	119660604	T	C
rs74992754	20622878	57057	TBX20	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31100249	C	A
rs753725	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30923094	T	C
rs7572482	23001997	6775	STAT4	umls:C0004943	GWASCAT	Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.	0.366362715	2012	STAT4	2	191150346	A	G
rs7572482	20622878	6775	STAT4	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.366362715	2010	STAT4	2	191150346	A	G
rs7574070	23001997	6775	STAT4	umls:C0004943	GWASCAT	Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.	0.366362715	2012	STAT4	2	191145762	A	C
rs7574070	23291587	6775	STAT4	umls:C0004943	GWASCAT	Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.	0.366362715	2013	STAT4	2	191145762	A	C
rs7574070	26097239	1230	CCR1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120814326	2015	STAT4	2	191145762	A	C
rs7574070	26097239	101928376	IL12A-AS1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120271442	2015	STAT4	2	191145762	A	C
rs75893422	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	NA	NA	NA	NA
rs7616215	26097239	101928376	IL12A-AS1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120271442	2015	LOC105377067	3	46164194	C	T
rs7616215	26097239	1230	CCR1	umls:C0004943	BeFree	Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ).	0.120814326	2015	LOC105377067	3	46164194	C	T
rs7631551	20622878	2829	XCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LOC105377067	3	46144818	C	A
rs7634425	20622878	23101	MCF2L2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	MCF2L2	3	183302804	T	C
rs76546355	25889189	3106	HLA-B	umls:C0004943	BeFree	We found that the HLA-B51 allele and the rs76546355/rs116799036 MHC SNP are independent genetic risk factors for BD in Iranian, and that positivity for the rs76546355/rs116799036 risk allele, but not for B51, does correlate with specific demographic characteristics or clinical manifestations in BD patients.	0.346098146	2015	NA	6	31381371	G	A
rs7731137	20622878	9421	HAND1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	5	154626094	T	G
rs7759666	20622878	5514	PPP1R10	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	PPP1R10	6	30601712	C	T
rs7760698	20622878	100130889	PSORS1C3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31182448	T	A
rs7854303	22039410	29126	CD274	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1LG2	9	5557672	T	C
rs7854303	22039410	5133	PDCD1	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1LG2	9	5557672	T	C
rs7854303	22039410	80380	PDCD1LG2	umls:C0004943	BeFree	None of the currently studied SNPs, PD-1 rs2227981 and rs10204525, PD-L1 rs1970000 and PD-L2 rs7854303, are associated with the susceptibility to Behcet's disease in a Chinese Han population.	0.000271442	2011	PDCD1LG2	9	5557672	T	C
rs80077509	20622878	394263	MUC21	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	NA	NA	NA	NA
rs897200	23001997	6775	STAT4	umls:C0004943	GWASCAT	Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.	0.366362715	2012	STAT4	2	191153045	T	C
rs915664	20622878	8870	IER3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	LINC00243	6	30826840	T	C
rs924080	20622878	149233	IL23R	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.130358398	2010	NA	1	67294457	T	C
rs9258966	20622878	3135	HLA-G	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.007729856	2010	NA	6	29872605	C	T
rs9261434	20622878	11074	TRIM31	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	30119999	G	C
rs9261547	20622878	7726	TRIM26	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	TRIM26	6	30187151	G	A
rs9261588	20622878	7726	TRIM26	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	HCG17	6	30243030	T	G
rs9262122	20622878	5514	PPP1R10	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	PPP1R10	6	30606065	T	C
rs9262152	20622878	9656	MDC1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	MDC1;MDC1-AS1	6	30713139	C	T
rs9262288	20622878	57176	VARS2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	VARS2	6	30917862	A	G
rs9262648	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31061396	C	A
rs9262651	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31061678	C	T
rs9262656	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31066487	A	G
rs9263733	20622878	170680	PSORS1C2	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	PSORS1C2	6	31141052	C	T
rs9263749	20622878	54535	CCHCR1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CCHCR1	6	31146738	G	A
rs9263794	20622878	6941	TCF19	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	TCF19	6	31162242	A	G
rs9263800	20622878	5460	POU5F1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	POU5F1	6	31166822	G	A
rs9263827	20622878	100130889	PSORS1C3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31181268	C	T
rs9263827	20622878	223117	SEMA3D	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31181268	C	T
rs9263844	20622878	100130889	PSORS1C3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31187409	C	T
rs9263948	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31213248	C	T
rs936551	20622878	10815	CPLX1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	CPLX1	4	827702	A	G
rs9380215	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31081878	G	A
rs9391709	20622878	285834	HCG22	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31109628	G	C
rs9468898	20622878	253018	HCG27	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	6	31214606	A	G
rs9501063	20622878	5460	POU5F1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	POU5F1	6	31166117	G	A,C
rs9798281	20622878	51665	ASB1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	NA	2	238811685	T	C
rs9819066	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71473959	C	T
rs9828629	20622878	27086	FOXP1	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002367032	2010	FOXP1	3	71481195	C	T
rs9990343	20622878	1232	CCR3	umls:C0004943	GAD	[Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease.]	0.002909916	2010	NA	3	46298321	A	G

GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)

GWASdb Snp Trait(Total Genotypes:396)
CHR	POS	SNPID	REF	ALT	ORI_SNPID	PMID	P_VALUE	P_VALUE_TEXT	OR/BETA	CI95_TEXT	GWAS_INITIAL_SAMPLE_SIZE	SUB_POPULATION	SUPER_POPULATION	GWAS_TRAIT	HPO_ID	HPO_TERM	DO_ID	DO_TERM	MESH_ID	MESH_TERM	EFO_ID	EFO_TERM	DOLITE_TERM	RISK_ALLELE	PUBLICATION_TYPE	AA	GENE_SYMBOL	TYPE	REFGENE
1	40049104	rs11206377	A	G	rs11206377	19442274	3.00E-04	Beh?et's disease	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	A
1	40049104	rs11206377	A	G	rs11206377	19442274	7.00E-04	Beh?et's disease(Eye disease absent)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	A
1	40049104	rs11206377	A	G	rs11206377	19442274	7.00E-04	Beh?et's disease(Neither eye nor vascular disease present)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	A
1	67744601	rs6660226	G	A	rs6660226	23291587	1.08E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
1	67753353	rs1495966	T	C	rs1495966	pha002888	6.09E-05	phs000272	1.25	[1.12-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
1	67753508	rs1495965	C	T	rs1495965	20622879	2.00E-11	NA	1.35	[1.24-1.47]	611 Japanese cases; 737 Japanese controls	Japanese(1348)	ALL(1348)	ASN(1348)	ALL(1348)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs1495965-G	Research Support, Non-U.S. Gov't	Comment	G
1	67753508	rs1495965	C	T	rs1495965	pha002888	6.99E-05	phs000272	1.25	[1.12-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
1	67760140	rs924080	T	C	rs924080	20622878	7.00E-09	NA	1.28	[1.18-1.39]	1,215 Turkish cases; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
1	67760140	rs924080	T	C	rs924080	23291587	5.36E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
1	67760140	rs924080	T	C	rs924080	pha002888	5.35E-06	phs000272	1.32	[1.16-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
1	206944645	rs1518111	T	C	rs1518111	20622878	4.00E-18	NA	1.45	[1.34-1.58]	1,215 Turkish cases; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
1	206945311	rs3024490	A	C	rs3024490	23291587	3.02E-07	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
1	206945311	rs3024490	A	C	rs3024490	pha002888	2.22E-07	phs000272	1.36	[1.21-1.53]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	IL10	intron	NM_000572
1	206946634	rs1800871	A	G	rs1800871	20622879	1.00E-14	NA	1.45	[1.32-1.60]	611 Japanese cases; 737 Japanese controls	Japanese(1348)	ALL(1348)	ASN(1348)	ALL(1348)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs1800871-T	Research Support, Non-U.S. Gov't	Comment	C
1	206946634	rs1800871	A	G	rs1800871	23291587	3.02E-07	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
2	102618370	rs4851526	A	G	rs4851526	pha002888	4.39E-05	phs000272	1.28	[1.14-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	IL1R2	intron	NM_004633
2	122018763	rs17006292	C	A	rs17006292	23001997	5.00E-09	NA	4.17	[2.50-5.00]	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	TFCP2L1
2	192010488	rs7574070	A	C	rs7574070	23001997	4.00E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	STAT4
2	192010488	rs7574070	A	C	rs7574070	23291587	1.00E-09	NA	1.27	[1.17-1.37]	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs7574070-A	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
2	192015072	rs7572482	A	G	rs7572482	23001997	4.00E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	STAT4
2	192015072	rs7572482	A	G	rs7572482	23291587	2.92E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
2	192015072	rs7572482	A	G	rs7572482	pha002888	3.18E-05	phs000272	1.27	[1.13-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	STAT4	intron	NM_003151
2	192017771	rs897200	T	C	rs897200	23001997	6.00E-09	NA	1.45	[1.30-1.60]	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	STAT4
2	235425433	rs10177805	T	C	rs10177805	23291587	2.49E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
2	239720326	rs9798281	T	C	rs9798281	pha002888	3.87E-05	phs000272	1.49	[1.23-1.82]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
3	33413263	rs4678929	T	G	rs4678929	23291587	1.73E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33419422	rs2291897	C	T	rs2291897	23291587	1.47E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33419422	rs2291897	C	T	rs2291897	pha002888	1.82E-05	phs000272	1.39	[1.19-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	FBXL2	intron	NM_012157
3	33421178	rs4045539	A	C	rs4045539	23291587	1.56E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33472937	rs1807844	T	C	rs1807844	23291587	2.13E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33472937	rs1807844	T	C	rs1807844	pha002888	5.56E-05	phs000272	1.35	[1.16-1.56]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	UBP1	intron	NM_014517
3	33479982	rs1357540	T	C	rs1357540	23291587	2.13E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33479982	rs1357540	T	C	rs1357540	pha002888	2.69E-05	phs000272	1.37	[1.19-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	UBP1	intron	NM_014517
3	33545785	rs6781484	T	C	rs6781484	23291587	4.66E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33592572	rs12487660	T	G	rs12487660	23291587	2.90E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	33592572	rs12487660	T	G	rs12487660	pha002888	2.70E-05	phs000272	1.32	[1.16-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	CLASP2	intron	NM_015097
3	45916222	rs12639224	C	T	rs12639224	pha002888	7.43E-05	phs000272	1.28	[1.14-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
3	46031957	rs2133660	C	T	rs2133660	pha002888	8.02E-05	phs000272	1.27	[1.12-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	FYCO1	intron	NM_024513
3	46180416	rs10510749	C	T	rs10510749	23291587	2.63E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	46180416	rs10510749	C	T	rs10510749	pha002888	4.22E-05	phs000272	1.43	[1.20-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
3	46186310	rs7631551	C	A	rs7631551	pha002888	7.95E-05	phs000272	1.41	[1.19-1.67]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
3	46205686	rs7616215	C	T	rs7616215	23291587	4.00E-13	NA	1.39	[1.27-1.52]	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs7616215-C	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	46339812	rs9990343	A	G	rs9990343	23291587	1.87E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	46339812	rs9990343	A	G	rs9990343	pha002888	2.76E-05	phs000272	1.3	[1.15-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
3	65148621	rs10510933	G	A	rs10510933	pha002888	3.46E-05	phs000272	1.32	[1.16-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
3	71517643	rs11706279	T	C	rs11706279	23291587	9.30E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71523110	rs9819066	C	T	rs9819066	23291587	7.07E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71523110	rs9819066	C	T	rs9819066	pha002888	4.55E-06	phs000272	1.31	[1.17-1.46]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	FOXP1	intron	NM_032682
3	71529915	rs6549391	A	C	rs6549391	23291587	1.32E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71530346	rs9828629	C	T	rs9828629	23291587	1.42E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71530346	rs9828629	C	T	rs9828629	pha002888	8.89E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	FOXP1	intron	NM_032682
3	71538696	rs6549392	G	T	rs6549392	pha002888	2.33E-05	phs000272	1.29	[1.15-1.46]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	FOXP1	intron	NM_032682
3	71545170	rs11720523	C	A	rs11720523	pha002888	2.09E-05	phs000272	1.29	[1.15-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	FOXP1	intron	NM_032682
3	71546744	rs6789751	T	C	rs6789751	23291587	1.15E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71549639	rs6779258	T	C	rs6779258	pha002888	1.11E-05	phs000272	1.3	[1.16-1.46]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	FOXP1	intron	NM_032682
3	71595258	rs11720121	T	C	rs11720121	23291587	2.76E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71595258	rs11720121	T	C	rs11720121	pha002888	1.28E-05	phs000272	1.3	[1.15-1.46]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	FOXP1	intron	NM_032682
3	71606466	rs6549400	T	G	rs6549400	23291587	1.85E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	71606466	rs6549400	T	G	rs6549400	pha002888	8.46E-06	phs000272	1.3	[1.16-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	FOXP1	intron	NM_032682
3	71672306	rs10460943	C	T	rs10460943	pha002888	7.33E-05	phs000272	1.37	[1.18-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
3	72514676	rs10049211	T	C	rs10049211	23291587	5.11E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	72514676	rs10049211	T	C	rs10049211	pha002888	5.35E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
3	72515960	rs11128275	G	A	rs11128275	pha002888	3.80E-05	phs000272	1.27	[1.14-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
3	121710086	rs11718322	G	A	rs11718322	pha002888	8.23E-05	phs000272	1.26	[1.12-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	ILDR1	intron	NM_175924
3	143604632	rs17275413	G	C	rs17275413	23041938	0.00000449	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	NA
3	149251359	rs10513355	A	G	rs10513355	pha002888	4.66E-05	phs000272	1.49	[1.23-1.80]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	WWTR1	intron	NM_015472
3	159630084	rs17809756	G	A	rs17809756	23291587	1.20E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	159665050	rs17810546	A	G	rs17810546	23291587	6.00E-07	All Turkish cases	1.55	[1.30-1.85]	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs17810546-A	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	159665050	rs17810546	A	G	rs17810546	pha002888	1.49E-05	phs000272	1.63	[1.30-2.03]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
3	159952278	rs6441306	A	G	rs6441306	pha002888	3.52E-05	phs000272	1.27	[1.13-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
3	183020592	rs7634425	T	C	rs7634425	23291587	2.63E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
3	183020592	rs7634425	T	C	rs7634425	pha002888	2.97E-05	phs000272	1.32	[1.15-1.49]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	MCF2L2	intron	NM_015078
3	183024519	rs1010769	T	G	rs1010769	23291587	2.26E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
4	821490	rs936551	A	G	rs936551	23291587	1.11E-07	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
4	821490	rs936551	A	G	rs936551	pha002888	5.29E-08	phs000272	1.37	[1.22-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
4	69177408	rs10033058	C	G	rs10033058	23041938	0.00000238	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	YTHDC1
4	69178920	rs2293595	T	C	rs2293595	23041938	0.00000461	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	YTHDC1
4	69183791	rs17089267	A	G	rs17089267	23041938	0.00000332	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	YTHDC1
4	136694463	rs2018601	T	C	rs2018601	23291587	2.36E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
4	154643503	rs1869947	G	A	rs1869947	23291587	2.41E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
4	176837789	rs1495714	C	A	rs1495714	23291587	1.78E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
4	176837789	rs1495714	C	A	rs1495714	pha002888	1.93E-05	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	GPM6A	intron	NM_201592
4	176872920	rs4690647	G	A	rs4690647	23291587	1.10E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
4	176872920	rs4690647	G	A	rs4690647	pha002888	1.13E-05	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	GPM6A	intron	NM_201592
5	6521837	rs563624	A	C	rs563624	pha002888	6.12E-05	phs000272	1.26	[1.12-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
5	54160345	rs4865879	C	T	rs4865879	pha002888	6.81E-05	phs000272	1.25	[1.12-1.40]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
5	54174906	rs10940434	T	C	rs10940434	pha002888	3.27E-05	phs000272	1.27	[1.13-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
5	96118866	rs17482078	C	T	rs17482078	23291587	4.00E-08	All Turkish cases - Recessive Model	3.08	[2.04-4.65]	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs17482078-T	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
5	96118866	rs17482078	C	T	rs17482078	23291587	5.00E-11	Turkish cases with Uveitis - Recessive Model	4.56	[2.88-7.22]	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs17482078-T	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
5	142974644	rs11167821	A	G	rs11167821	pha002888	7.98E-05	phs000272	1.37	[1.18-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
5	154005654	rs7731137	T	G	rs7731137	23291587	1.73E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
5	154005654	rs7731137	T	G	rs7731137	pha002888	9.50E-05	phs000272	1.26	[1.12-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
5	167838237	rs1965673	C	G	rs1965673	23041938	0.000000491	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	WWC1
5	167838336	rs1465400	G	C	rs1465400	23041938	0.00000158	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	WWC1
6	15260153	rs11962776	C	A	rs11962776	pha002888	3.94E-05	phs000272	1.67	[1.30-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	JARID2	intron	NM_004973
6	29539765	rs3025652	G	A	rs3025652	pha002888	6.81E-05	phs000272	1.35	[1.16-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	29611885	rs3131854	T	C	rs3131854	pha002888	2.54E-08	phs000272	1.49	[1.30-1.72]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G,A	NA	NA	NA
6	29628437	rs3135050	T	C	rs3135050	pha002888	2.42E-11	phs000272	1.82	[1.52-2.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	MOG	intron	NM_002433
6	29635928	rs2071653	T	C	rs2071653	pha002888	2.34E-07	phs000272	1.47	[1.27-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	MOG	intron	NM_002433
6	29673483	rs3131863	G	A	rs3131863	pha002888	5.63E-06	phs000272	1.33	[1.18-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	29691019	rs1362126	G	A	rs1362126	pha002888	7.54E-06	phs000272	1.29	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	HLA-F	nearGene-5	NM_001098478
6	29700079	rs2523399	C	T	rs2523399	pha002888	2.37E-06	phs000272	1.32	[1.18-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	HLA-F-AS1	intron	NR_026972
6	29703262	rs2394160	A	G	rs2394160	pha002888	7.92E-05	phs000272	1.25	[1.12-1.40]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	HLA-F-AS1	intron	NR_026972
6	29708222	rs1610603	T	C	rs1610603	pha002888	1.24E-08	phs000272	1.61	[1.37-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	HLA-F-AS1	intron	NR_026972
6	29710726	rs4713240	A	G	rs4713240	pha002888	5.79E-05	phs000272	1.31	[1.15-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	HLA-F-AS1	intron	NR_026972
6	29712866	rs1633091	T	C	rs1633091	pha002888	1.94E-08	phs000272	1.59	[1.35-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	HLA-F-AS1	intron	NR_026972
6	29715332	rs34260811	C	A	rs34260811	pha002888	7.25E-05	phs000272	1.31	[1.14-1.49]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	HLA-F-AS1	intron	NR_026972
6	29721146	rs4713244	G	A	rs4713244	pha002888	5.46E-05	phs000272	1.31	[1.15-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	29721755	rs1611297	C	T	rs74728727	pha002888	1.20E-08	phs000272	1.61	[1.37-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	29724310	rs1633068	T	C	rs79887596	pha002888	1.28E-08	phs000272	1.61	[1.37-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	29728209	rs113795410	C	A	rs113795410	pha002888	1.28E-08	phs000272	1.61	[1.37-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	29729286	rs1610630	C	T	rs1610630	pha002888	1.18E-08	phs000272	1.61	[1.37-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	29730642	rs1633048	A	G	rs1633048	pha002888	5.53E-09	phs000272	1.61	[1.37-1.92]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	29732969	rs1737060	G	C	rs1737060	pha002888	2.43E-09	phs000272	1.64	[1.39-1.92]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	29735693	rs1737046	A	G	rs1737046	pha002888	1.12E-05	phs000272	1.3	[1.16-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	29755451	rs2743941	T	C	rs2743941	pha002888	4.43E-07	phs000272	1.43	[1.23-1.64]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	29787072	rs2743931	C	T	rs2743931	pha002888	3.71E-11	phs000272	1.89	[1.56-2.27]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	29823606	rs3132726	A	G	rs3132726	pha002888	2.93E-06	phs000272	1.37	[1.20-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C,T	NA	NA	NA
6	29839816	rs3094654	T	C	rs3094654	pha002888	1.17E-05	phs000272	1.28	[1.15-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	29840382	rs9258966	C	T	rs9258966	pha002888	1.02E-05	phs000272	1.3	[1.15-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C,G	NA	NA	NA
6	29917439	rs2517715	T	C	rs74976521	pha002888	1.44E-06	phs000272	1.34	[1.19-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	29933881	rs6457110	T	A	rs6457110	pha002888	1.88E-07	phs000272	1.35	[1.21-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	29934697	rs4713270	G	A	rs4713270	pha002888	2.37E-06	phs000272	1.34	[1.19-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	29940750	rs2256919	C	A	rs2256919	pha002888	2.67E-05	phs000272	1.27	[1.14-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	29943067	rs6904029	G	A	rs6904029	pha002888	2.06E-06	phs000272	1.35	[1.19-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	29954364	rs4947244	C	G	rs4947244	pha002888	1.92E-06	phs000272	1.36	[1.20-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	29955199	rs5025708	G	T	rs5025708	pha002888	9.16E-11	phs000272	1.92	[1.59-2.38]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	29984252	rs9357092	G	A	rs9357092	pha002888	3.85E-07	phs000272	1.38	[1.22-1.57]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	ZNRD1-AS1	intron	NR_026751
6	30008996	rs9261212	C	T	rs9261212	pha002888	2.95E-10	phs000272	1.85	[1.54-2.27]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	ZNRD1-AS1	intron	NR_026751
6	30047403	rs4711209	G	A	rs4711209	pha002888	1.03E-06	phs000272	1.37	[1.21-1.55]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30087776	rs9261434	G	C	rs9261434	pha002888	1.75E-06	phs000272	1.64	[1.33-2.04]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30154928	rs9261547	G	A	rs9261547	pha002888	5.94E-05	phs000272	1.52	[1.23-1.85]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	TRIM26	intron	NM_003449
6	30176122	rs10947058	C	T	rs10947058	pha002888	2.60E-06	phs000272	1.58	[1.31-1.92]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	TRIM26	intron	NM_003449
6	30206186	rs10456378	G	A	rs10456378	pha002888	1.04E-06	phs000272	1.62	[1.33-1.97]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30210807	rs9261588	T	G	rs9261588	pha002888	3.46E-05	phs000272	1.54	[1.25-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30282332	rs3094065	T	C	rs3094065	pha002888	1.81E-06	phs000272	1.67	[1.35-2.08]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	HCG18	intron	NR_024052
6	30334339	rs2040450	C	T	rs2040450	pha002888	9.99E-05	phs000272	1.32	[1.15-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30430482	rs2516676	G	C	rs2516676	pha002888	2.06E-06	phs000272	1.56	[1.30-1.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30433611	rs2524172	A	G	rs2524172	pha002888	4.65E-06	phs000272	1.64	[1.33-2.04]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30455920	rs1264459	G	A	rs1264459	pha002888	4.51E-06	phs000272	1.52	[1.27-1.82]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T,C	LOC100653026	intron	XR_132912
6	30569489	rs7759666	C	T	rs7759666	pha002888	3.61E-05	phs000272	1.32	[1.16-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	PPP1R10	intron	NM_002714
6	30573842	rs9262122	T	C	rs9262122	pha002888	4.72E-05	phs000272	1.31	[1.15-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	PPP1R10	intron	NM_002714
6	30680916	rs9262152	C	T	rs9262152	pha002888	3.62E-05	phs000272	1.32	[1.16-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	MDC1	missense	NM_014641
6	30760639	rs34682678	A	C	rs34682678	pha002888	1.68E-05	phs000272	1.42	[1.21-1.67]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	30776590	rs1264362	C	G	rs1264362	pha002888	1.31E-05	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30794617	rs915664	T	C	rs915664	pha002888	8.45E-05	phs000272	1.26	[1.12-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	30816270	rs2535331	G	A	rs2535331	pha002888	3.74E-06	phs000272	1.3	[1.16-1.46]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30821187	rs2250264	G	A	rs2250264	pha002888	8.16E-09	phs000272	1.41	[1.25-1.58]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	30826904	rs2535327	T	C	rs2535327	pha002888	1.30E-07	phs000272	1.35	[1.21-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	30838688	rs2844654	T	G	rs2844654	pha002888	4.43E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	30844314	rs1264333	T	C	rs1264333	pha002888	4.42E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	30845563	rs1264332	G	C	rs1264332	pha002888	4.98E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30846830	rs1264331	G	T	rs1264331	pha002888	4.47E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30850582	rs1264327	G	A	rs1264327	pha002888	1.68E-07	phs000272	1.35	[1.21-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T,C	DDR1	nearGene-5	NM_013993
6	30882513	rs1264303	A	G	rs1264303	pha002888	7.62E-06	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	VARS2	intron	NM_020442
6	30882634	rs1264302	C	T	rs1264302	pha002888	7.39E-06	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	VARS2	cds-synon	NM_020442
6	30882781	rs1264301	G	T	rs1264301	pha002888	7.62E-06	phs000272	1.16	[1.03-1.30]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	VARS2	cds-synon	NM_020442
6	30884436	rs1264298	A	G	rs1264298	pha002888	7.62E-06	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	VARS2	intron	NM_020442
6	30885639	rs9262288	A	G	rs9262288	pha002888	6.65E-06	phs000272	1.29	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	VARS2	intron	NM_020442
6	30886350	rs9262293	C	G	rs75893422	pha002888	8.03E-06	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	VARS2	intron	NM_020442
6	30889260	rs2517467	G	A	rs2517467	pha002888	2.25E-05	phs000272	1.3	[1.15-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	VARS2	intron	NM_020442
6	30890483	rs2074506	G	T	rs2074506	pha002888	5.71E-06	phs000272	1.3	[1.16-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	VARS2	missense	NM_020442
6	30890871	rs753725	T	C	rs753725	pha002888	2.01E-05	phs000272	1.3	[1.15-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	VARS2	intron	NM_020442
6	30893831	rs2532938	G	A	rs2532938	pha002888	7.71E-06	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	VARS2	intron	NM_020442
6	30894759	rs2532934	G	A	rs2532934	pha002888	2.37E-05	phs000272	1.3	[1.15-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	30897774	rs2532929	A	G	rs2532929	pha002888	1.51E-05	phs000272	1.28	[1.15-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30898687	rs2844652	C	T	rs2844652	pha002888	7.62E-06	phs000272	1.29	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	SFTA2	nearGene-3	NM_205854
6	30920890	rs2240804	G	A	rs2240804	pha002888	2.09E-07	phs000272	1.35	[1.20-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	DPCR1	missense	NM_080870
6	30932309	rs2844697	C	T	rs2844697	pha002888	6.16E-08	phs000272	1.47	[1.28-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	30933794	rs3095089	G	T	rs3095089	pha002888	1.03E-05	phs000272	1.69	[1.33-2.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30946496	rs2844680	T	G	rs2844680	pha002888	6.06E-07	phs000272	1.33	[1.19-1.49]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	30960267	rs2517411	T	C	rs2517411	23041938	0.000000825	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
6	30999703	rs17190071	G	A	rs17190071	pha002888	1.55E-05	phs000272	1.35	[1.18-1.55]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	MUC22	intron	NM_001198815
6	31010200	rs2508015	G	A	rs80077509	pha002888	3.09E-06	phs000272	1.33	[1.18-1.49]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31016978	rs2251830	C	A	rs2251830	pha002888	2.52E-06	phs000272	1.32	[1.18-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31018546	rs2523864	C	T	rs2523864	pha002888	1.96E-06	phs000272	1.32	[1.18-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A,G	NA	NA	NA
6	31029173	rs9262648	C	A	rs9262648	pha002888	4.11E-05	phs000272	1.28	[1.14-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31029455	rs9262651	C	T	rs9262651	pha002888	7.50E-05	phs000272	1.26	[1.13-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31032042	rs2394423	G	A	rs2394423	pha002888	4.84E-05	phs000272	1.27	[1.13-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31034264	rs9262656	A	G	rs9262656	pha002888	4.80E-05	phs000272	1.27	[1.13-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31049655	rs9380215	G	A	rs9380215	pha002888	6.13E-23	phs000272	2.08	[1.79-2.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31051553	rs9380217	C	T	rs9380217	23001997	1.98E-11	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
6	31058178	rs4947296	T	C	rs4947296	23001997	1.00E-11	NA	2.57	[1.96-3.37]	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
6	31058178	rs4947296	T	C	rs4947296	23041938	4.01E-13	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
6	31058178	rs4947296	T	C	rs4947296	pha002888	2.37E-23	phs000272	2.1	[1.81-2.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31067009	rs2517403	T	C	rs2517403	pha002888	3.72E-06	phs000272	1.32	[1.18-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A,G	NA	NA	NA
6	31071058	rs2508011	A	C	rs2508011	pha002888	3.21E-06	phs000272	1.32	[1.18-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31075481	rs2844635	A	G	rs2844635	pha002888	2.76E-06	phs000272	1.32	[1.18-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31077405	rs9391709	G	C	rs9391709	pha002888	1.38E-20	phs000272	1.95	[1.69-2.25]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31078005	rs1265062	C	T	rs1265062	pha002888	5.95E-06	phs000272	1.3	[1.16-1.47]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31080828	rs2233967	C	G	rs2233967	pha002888	9.71E-11	phs000272	1.52	[1.34-1.73]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	C6orf15	nearGene-5	NM_014070
6	31080899	rs2233965	T	G	rs2233965	pha002888	1.23E-10	phs000272	1.52	[1.34-1.73]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A,C	C6orf15	nearGene-5	NM_014070
6	31082081	rs17190526	G	A	rs17190526	pha002888	8.55E-06	phs000272	1.72	[1.35-2.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	C6orf15	nearGene-5	NM_014070
6	31082361	rs6917517	C	T	rs6917517	pha002888	4.73E-12	phs000272	1.52	[1.35-1.71]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	PSORS1C1	nearGene-5	NM_014068
6	31084435	rs1062470	G	A	rs1062470	pha002888	8.99E-05	phs000272	1.28	[1.12-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	CDSN	cds-synon	NM_001264
6	31087133	rs3095324	C	T	rs3095324	23001997	4.24E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	CDSN
6	31087133	rs386579334	C	T	rs3095324	23001997	4.24E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	CDSN
6	31092124	rs3778638	G	A	rs3778638	pha002888	7.58E-05	phs000272	1.33	[1.15-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	PSORS1C1	intron	NM_014068
6	31092124	rs527680481	G	A	rs3778638	pha002888	7.58E-05	phs000272	1.33	[1.15-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	PSORS1C1	intron	NM_014068
6	31099577	rs4959053	G	A	rs4959053	23001997	2.00E-20	NA	4.38	[3.20-5.99]	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	PSORS1C1
6	31099577	rs4959053	G	A	rs4959053	23041938	2.08E-11	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	PSORS1C1
6	31105633	rs2074478	C	T	rs2074478	pha002888	1.09E-07	phs000272	1.49	[1.29-1.73]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A,G	PSORS1C2	UTR-3	NM_014069
6	31108829	rs9263733	C	T	rs9263733	pha002888	3.63E-09	phs000272	2.5	[1.82-3.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	PSORS1C2	nearGene-5	NM_014069
6	31112354	rs11967883	C	T	rs11967883	pha002888	3.15E-06	phs000272	1.83	[1.41-2.36]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	CCHCR1	intron	NM_019052
6	31113703	rs17196989	A	G	rs17196989	pha002888	3.96E-10	phs000272	2.23	[1.73-2.89]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	CCHCR1	intron	NM_019052
6	31114515	rs9263749	G	A	rs9263749	pha002888	5.60E-05	phs000272	1.39	[1.18-1.64]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	CCHCR1	intron	NM_019052
6	31116627	rs3131014	G	A	rs113481038	pha002888	8.56E-14	phs000272	1.58	[1.40-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	CCHCR1	intron	NM_019052
6	31122997	rs2073716	C	G	rs2073716	23001997	4.56E-09	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	CCHCR1
6	31130019	rs9263794	A	G	rs9263794	pha002888	9.83E-05	phs000272	1.41	[1.18-1.67]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	TCF19	intron	NM_001077511
6	31133894	rs9501063	G	C	rs9501063	pha002888	2.29E-05	phs000272	1.68	[1.32-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	POU5F1	UTR-5	NM_203289
6	31134599	rs9263800	G	A	rs9263800	pha002888	6.55E-05	phs000272	1.43	[1.19-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	POU5F1	UTR-5	NM_203289
6	31134888	rs3130931	T	C	rs3130931	pha002888	1.14E-05	phs000272	1.32	[1.17-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	POU5F1	intron	NM_002701
6	31135735	rs200484944	A	AC	rs113112186	pha002888	2.97E-05	phs000272	1.32	[1.16-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	POU5F1	intron	NM_002701
6	31135735	rs9263805	A	C	rs113112186	pha002888	2.97E-05	phs000272	1.32	[1.16-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	POU5F1	intron	NM_002701
6	31149045	rs9263827	C	T	rs9263827	pha002888	1.39E-07	phs000272	2.08	[1.59-2.78]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31150225	rs7760698	T	A	rs7760698	pha002888	4.92E-05	phs000272	1.47	[1.22-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31155186	rs9263844	C	T	rs9263844	pha002888	8.05E-11	phs000272	1.49	[1.33-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31162154	rs28362332	G	A	rs28362332	pha002888	1.02E-05	phs000272	1.37	[1.19-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31165527	rs28362343	G	A	rs28362343	pha002888	1.38E-05	phs000272	1.37	[1.19-1.56]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	HCG27	nearGene-5	NR_026791
6	31173096	rs4446605	A	G	rs4446605	pha002888	1.42E-05	phs000272	1.37	[1.19-1.56]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31181025	rs9263948	C	T	rs9263948	pha002888	8.67E-06	phs000272	1.37	[1.19-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31182383	rs9468898	A	G	rs9468898	pha002888	2.51E-06	phs000272	1.63	[1.33-2.00]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31187075	rs3130467	C	T	rs3130467	pha002888	5.92E-06	phs000272	1.33	[1.17-1.50]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31196671	rs3130944	C	G	rs3130944	23041938	0.00000142	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	NA
6	31199208	rs3130473	C	T	rs3130473	pha002888	1.86E-08	phs000272	1.43	[1.26-1.62]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31206868	rs2894186	G	C	rs2894186	23041938	0.00000408	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	NA
6	31218835	rs4084090	A	G	rs4084090	pha002888	2.86E-09	phs000272	1.79	[1.47-2.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31235798	rs3873372	G	T	rs113198053	pha002888	1.61E-07	phs000272	1.8	[1.44-2.25]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31243884	rs3130696	G	A	rs111614996	pha002888	7.62E-05	phs000272	1.28	[1.13-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31250606	rs9468914	A	C	rs9468914	pha002888	1.37E-13	phs000272	1.52	[1.37-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31254088	rs2853933	T	C	rs2853933	pha002888	9.13E-07	phs000272	1.37	[1.20-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31256753	rs2524044	T	G	rs2524044	pha002888	1.93E-05	phs000272	1.39	[1.19-1.62]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31258141	rs28367594	G	A	rs28367594	pha002888	7.32E-08	phs000272	1.79	[1.45-2.22]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31261276	rs2243868	A	G	rs2243868	pha002888	9.44E-07	phs000272	1.37	[1.20-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31272463	rs9368678	T	C	rs9368678	23041938	9.76E-08	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
6	31273745	rs3873386	T	C	rs3873386	pha002888	1.00E-05	phs000272	1.28	[1.15-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31318164	rs4394274	C	A	rs4394274	23001997	1.40E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
6	31321685	rs1058026	A	C	rs78586586	pha002888	1.31E-27	phs000272	1.86	[1.67-2.09]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	HLA-B	UTR-3	NM_005514
6	31326960	rs2523591	G	A	rs2523591	pha002888	4.54E-14	phs000272	1.59	[1.41-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	HLA-B	nearGene-5	NM_005514
6	31331829	rs2523554	C	T	rs2523554	pha002888	3.34E-11	phs000272	1.67	[1.43-1.96]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31333499	rs2523545	G	A	rs2523545	pha002888	2.95E-06	phs000272	1.43	[1.23-1.67]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31333562	rs2523544	G	A	rs2523544	pha002888	1.74E-08	phs000272	1.69	[1.41-2.04]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31335806	rs9266399	A	T	rs9266399	pha002888	1.55E-43	phs000272	2.28	[2.02-2.56]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31336418	rs9266406	G	A	rs9266406	23001997	2.00E-10	NA	2.29	[1.77-2.95]	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	NA
6	31336418	rs9266406	G	A	rs9266406	23041938	2.56E-10	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	NA
6	31336568	rs9266409	T	C	rs9266409	23001997	1.91E-10	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
6	31336568	rs9266409	T	C	rs9266409	23041938	2.56E-10	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
6	31336870	rs2253907	C	T	rs112243466	pha002888	1.70E-21	phs000272	1.72	[1.54-1.92]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31336870	rs2253907	C	T	rs2253907	23001997	1.78E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
6	31336870	rs2253907	C	T	rs2253907	23041938	5.87E-08	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
6	31340158	rs9266490	A	G	rs9266490	23001997	2.80E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
6	31340328	rs2523522	T	C	rs2523522	pha002888	2.27E-13	phs000272	1.54	[1.37-1.75]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31340559	rs2394990	C	A	rs2394990	pha002888	1.97E-13	phs000272	1.54	[1.37-1.75]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31343632	rs6933050	T	C	rs6933050	23041938	1.64E-10	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
6	31343827	rs6910516	A	G	rs6910516	23041938	2.56E-10	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	NA	NA
6	31345021	rs7382258	G	A	rs7382258	pha002888	1.58E-13	phs000272	1.54	[1.37-1.72]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31350704	rs1521	C	T	rs1521	pha002888	4.25E-08	phs000272	1.04	[0.92-1.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31352446	rs7775759	G	A	rs7775759	23041938	0.000000147	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	NA
6	31353593	rs2844529	G	A	rs2844529	pha002888	7.10E-13	phs000272	1.52	[1.35-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31354104	rs2428486	T	C	rs2428486	pha002888	7.10E-13	phs000272	1.52	[1.35-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31354560	rs13437082	C	T	rs13437082	pha002888	1.96E-07	phs000272	1.37	[1.22-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31354595	rs2596562	T	C	rs2596562	pha002888	7.10E-13	phs000272	1.52	[1.35-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31355119	rs13437088	C	T	rs13437088	pha002888	2.36E-07	phs000272	1.37	[1.22-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31360389	rs2523477	T	C	rs2523477	pha002888	1.30E-05	phs000272	1.61	[1.30-2.04]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	31360433	rs7751725	A	G	rs7751725	pha002888	4.70E-07	phs000272	1.35	[1.20-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31362930	rs2523467	C	T	rs2523467	pha002888	5.16E-13	phs000272	1.52	[1.35-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31368964	rs2844521	C	T	rs2844521	pha002888	4.96E-13	phs000272	1.52	[1.35-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	MICA	intron	NR_036524
6	31374262	rs2857281	A	C	rs2857281	pha002888	4.31E-05	phs000272	1.59	[1.27-1.96]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	MICA	intron	NM_001177519
6	31383848	rs3094584	G	A	rs3094584	23041938	0.00000019	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	NA	NA
6	31384479	rs2848713	G	A	rs2848713	pha002888	5.62E-45	phs000272	2.48	[2.18-2.82]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31384578	rs9468992	G	A	rs9468992	pha002888	3.76E-05	phs000272	1.39	[1.19-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31387373	rs2596530	G	A	rs2596530	pha002888	4.29E-08	phs000272	1.49	[1.30-1.72]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31388214	rs2844513	G	A	rs2844513	pha002888	1.69E-07	phs000272	1.37	[1.22-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31388595	rs9295993	A	G	rs9295993	pha002888	8.35E-07	phs000272	1.37	[1.20-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31389784	rs2844511	A	G	rs2844511	pha002888	5.36E-08	phs000272	1.49	[1.30-1.72]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31390203	rs10223568	T	C	rs10223568	pha002888	4.63E-05	phs000272	1.37	[1.18-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31392118	rs9501109	A	G	rs9501109	pha002888	3.64E-10	phs000272	1.49	[1.32-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31394700	rs2516472	A	G	rs2516472	pha002888	7.49E-06	phs000272	1.69	[1.35-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31401374	rs4346874	C	T	rs4346874	pha002888	9.20E-05	phs000272	1.37	[1.16-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31407643	rs7772549	T	C	rs7772549	pha002888	1.12E-08	phs000272	1.41	[1.25-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31407828	rs9469003	T	C	rs9469003	pha002888	4.39E-05	phs000272	1.39	[1.18-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31409024	rs9469007	T	C	rs9469007	pha002888	6.14E-09	phs000272	1.43	[1.27-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31409857	rs28575156	A	G	rs28575156	pha002888	3.76E-05	phs000272	1.39	[1.19-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31410597	rs3899823	G	A	rs3899823	pha002888	3.47E-08	phs000272	1.45	[1.27-1.64]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31416156	rs2516464	A	G	rs2516464	pha002888	2.21E-14	phs000272	1.56	[1.39-1.75]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31416536	rs2516463	A	G	rs2516463	pha002888	8.34E-06	phs000272	1.69	[1.33-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31416920	rs16899646	C	G	rs16899646	pha002888	1.25E-06	phs000272	1.45	[1.25-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31417396	rs9501129	T	C	rs9501129	pha002888	2.64E-06	phs000272	1.41	[1.22-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31419387	rs2516458	T	C	rs2516458	pha002888	1.95E-14	phs000272	1.56	[1.39-1.75]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31420018	rs2516456	T	C	rs2516456	pha002888	1.39E-14	phs000272	1.56	[1.41-1.75]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31421112	rs6919586	A	G	rs77993522	pha002888	1.11E-06	phs000272	1.45	[1.25-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31425033	rs2254386	T	C	rs2254386	pha002888	1.54E-14	phs000272	1.56	[1.39-1.75]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31425985	rs2596480	C	T	rs2596480	pha002888	8.06E-06	phs000272	1.69	[1.33-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31428967	rs2596472	G	A	rs2596472	pha002888	2.45E-05	phs000272	1.33	[1.16-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	HCP5	nearGene-5	NM_006674
6	31429927	rs3094228	T	C	rs3094228	pha002888	4.27E-12	phs000272	1.59	[1.41-1.82]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31432125	rs2284178	C	T	rs2284178	pha002888	3.06E-10	phs000272	1.43	[1.28-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	HCP5	UTR-3	NM_006674
6	31434111	rs3094604	A	G	rs3094604	pha002888	3.20E-09	phs000272	1.67	[1.41-1.96]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31435119	rs2516518	G	A	rs2516518	pha002888	3.31E-06	phs000272	1.67	[1.35-2.08]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31436047	rs2518028	T	C	rs2518028	pha002888	4.41E-08	phs000272	1.52	[1.32-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31442782	rs3131643	G	A	rs3131643	pha002888	6.47E-05	phs000272	1.67	[1.28-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	NA	NA	NA	NA
6	31474280	rs2242955	G	A	rs2242955	pha002888	1.56E-05	phs000272	1.43	[1.22-1.69]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	MICB	intron	NM_005931
6	31474688	rs3093953	T	G	rs3093953	23001997	3.45E-08	NA	NA	NA	147 Han Chinese cases; 951 Han Chinese controls	Han Chinese(1098)	ALL(1098)	ASN(1098)	ALL(1098)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	MICB
6	31484683	rs3131631	G	C	rs3131631	pha002888	4.39E-05	phs000272	1.47	[1.22-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31488145	rs3130637	A	G	rs3130637	pha002888	3.00E-05	phs000272	1.47	[1.23-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
6	31490725	rs3093993	C	A	rs3093993	pha002888	3.12E-05	phs000272	1.47	[1.22-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	31491000	rs3095227	A	G	rs3095227	pha002888	3.12E-05	phs000272	1.47	[1.22-1.79]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C,T	NA	NA	NA
6	31493421	rs3093986	T	A	rs3093986	pha002888	2.33E-06	phs000272	1.69	[1.35-2.08]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
6	31498497	rs3093978	C	A	rs3093978	pha002888	8.82E-07	phs000272	1.72	[1.39-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	DDX39B	intron	NM_004640
6	31501413	rs3093948	A	G	rs3093948	pha002888	8.72E-07	phs000272	1.72	[1.37-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	DDX39B	intron	NM_004640
6	31502861	rs3093976	A	G	rs3093976	pha002888	1.03E-06	phs000272	1.72	[1.37-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	DDX39B	intron	NM_004640
6	31504587	rs3130057	G	T	rs3130057	pha002888	1.07E-06	phs000272	1.72	[1.37-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	DDX39B	intron	NM_004640
6	31505887	rs3130058	T	C	rs3130058	pha002888	6.23E-07	phs000272	1.72	[1.39-2.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	DDX39B	intron	NM_004640
6	31506744	rs2516393	A	C	rs2516393	pha002888	8.82E-07	phs000272	1.72	[1.39-2.13]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	DDX39B	intron	NM_004640
6	31507447	rs2239709	C	T	rs2239709	pha002888	4.56E-05	phs000272	1.39	[1.19-1.63]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	DDX39B	intron	NM_004640
6	31511857	rs2251824	G	A	rs2251824	pha002888	5.97E-06	phs000272	1.4	[1.21-1.62]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	ATP6V1G2-DDX39B	intron	NR_037853
6	31512799	rs2071593	G	A	rs2071593	pha002888	4.56E-05	phs000272	1.39	[1.19-1.63]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	ATP6V1G2	UTR-3	NM_138282
6	31513559	rs2523503	C	A	rs2523503	pha002888	5.59E-06	phs000272	1.4	[1.21-1.62]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	ATP6V1G2	intron	NM_138282
6	31518354	rs2523500	G	A	rs2523500	pha002888	2.64E-06	phs000272	1.33	[1.18-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NFKBIL1	intron	NM_005007
6	31521302	rs2255798	G	C	rs2255798	pha002888	8.43E-05	phs000272	1.39	[1.18-1.63]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NFKBIL1	intron	NM_005007
6	31525448	rs2230365	C	T	rs2230365	pha002888	2.52E-05	phs000272	1.33	[1.16-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NFKBIL1	cds-synon	NM_005007
6	31538244	rs2009658	C	G	rs2009658	pha002888	6.64E-05	phs000272	1.34	[1.16-1.55]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	LOC100287329	intron	XR_132517
6	31540556	rs2229094	T	C	rs2229094	pha002888	1.68E-06	phs000272	1.34	[1.19-1.51]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	LTA	missense	NM_000595
6	31564821	rs2844480	C	T	rs2844480	pha002888	4.62E-06	phs000272	1.38	[1.20-1.58]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
6	32429894	rs9268861	C	A	rs9268861	23041938	0.000000666	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
6	32787570	rs2857106	T	C	rs2857106	pha002888	2.39E-05	phs000272	1.39	[1.19-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
6	137514790	rs4896243	C	T	rs4896243	pha002888	2.67E-05	phs000272	1.27	[1.14-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
7	7348633	rs10486156	C	T	rs10486156	23291587	2.15E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
7	7348633	rs10486156	C	T	rs10486156	pha002888	3.69E-06	phs000272	1.39	[1.22-1.61]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
7	20819770	rs2709748	G	A	rs2709748	pha002888	1.38E-05	phs000272	1.43	[1.22-1.68]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
7	29102308	rs317711	C	G	rs317711	19442274	1.00E-04	Beh?et's disease	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
7	29102308	rs317711	C	G	rs317711	19442274	3.00E-04	Beh?et's disease(Neither eye nor vascular disease present)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
7	29102308	rs317711	C	G	rs317711	19442274	4.00E-04	Beh?et's disease(Vascular disease absent)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
7	29102308	rs317711	C	G	rs317711	19442274	6.00E-04	Beh?et's disease(Eye disease absent)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
7	105658451	rs6967330	G	A	rs6967330	pha002888	8.43E-05	phs000272	1.32	[1.15-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	CDHR3	missense	NM_152750
7	111778425	rs13247109	T	C	rs13247109	23291587	1.75E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
7	111778586	rs13232973	C	T	rs13232973	23291587	2.26E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
7	150217309	rs3735080	C	T	rs3735080	23041938	0.0000461	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	G	GIMAP7
7	150230692	rs10277380	T	C	rs10277380	23041938	0.000000398	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
7	150231309	rs11769828	C	T	rs11769828	23041938	0.0000016	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
7	150233827	rs1916012	A	G	rs1916012	23041938	0.000000262	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
7	150235783	rs1522596	A	G	rs1522596	23041938	0.000000347	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
7	150245256	rs10236188	T	C	rs10236188	23041938	0.000000398	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
7	150247024	rs1608157	C	G	rs1608157	23041938	6.01E-08	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
7	150263761	rs2177188	G	A	rs2177188	23041938	0.0000354	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
7	150292545	rs6969250	C	T	rs6969250	23041938	0.0000562	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	NA
7	150326562	rs13226190	T	G	rs13226190	23041938	0.000059	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	T	GIMAP6
7	150349937	rs10266069	A	G	rs10266069	23041938	0.00000223	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
7	150350975	rs10256482	T	C	rs10256482	23041938	0.0000001	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
7	150389593	rs1860871	T	C	rs1860871	23041938	0.000228	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	GIMAP2
7	150392005	rs4725927	C	A	rs4725927	23041938	0.000231	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	NA
7	150418045	rs2286900	G	A	rs2286900	23041938	0.00000922	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	C	GIMAP1
8	4634415	rs6986423	G	T	rs6986423	pha002888	1.27E-05	phs000272	1.28	[1.15-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	CSMD1	intron	NM_033225
8	126328383	rs7004739	G	A	rs7004739	23291587	2.49E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
8	126328383	rs7004739	G	A	rs7004739	pha002888	2.14E-05	phs000272	1.27	[1.14-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NSMCE2	intron	NM_173685
9	90611872	rs10868677	C	T	rs10868677	pha002888	8.79E-05	phs000272	1.25	[1.12-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
9	100105782	rs2061634	C	G	rs2061634	19442274	3.01E-05	Beh?et's disease(Eye disease absent)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
9	100105782	rs2061634	C	G	rs2061634	19442274	4.20E-05	Beh?et's disease	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
9	100105782	rs2061634	C	G	rs2061634	19442274	6.22E-06	Beh?et's disease(Vascular disease absent)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
9	100105782	rs2061634	C	G	rs2061634	19442274	7.16E-06	Beh?et's disease(Neither eye nor vascular disease present)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	G
9	119172047	rs17302884	A	G	rs17302884	pha002888	5.16E-05	phs000272	1.28	[1.14-1.44]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
9	119181794	rs17303101	G	A	rs17303101	23291587	1.04E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
9	119248059	rs17220352	A	G	rs17220352	23291587	6.61E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
9	138559891	rs488709	G	A	rs488709	23291587	2.80E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
10	50109223	rs3849150	C	T	rs3849150	pha002888	2.73E-05	phs000272	1.34	[1.17-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	WDFY4	intron	NM_020945
11	86603490	rs10898549	A	G	rs10898549	23291587	1.65E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
11	122641086	rs4936742	T	C	rs4936742	19442274	7.60E-04	Beh?et's disease	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	T
11	122641086	rs4936742	T	C	rs4936742	19442274	8.00E-04	Beh?et's disease(Eye disease present)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	T
12	10529034	rs2617150	T	C	rs2617150	23291587	1.20E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
12	10560957	rs2617170	T	C	rs2617170	23291587	1.00E-09	NA	1.28	[1.18-1.39]	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	rs2617170-T	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
12	70385323	rs1882191	C	T	rs1882191	pha002888	7.52E-05	phs000272	1.3	[1.15-1.49]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
12	118431327	rs7295696	T	C	rs7295696	23291587	2.21E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
12	118431327	rs7295696	T	C	rs7295696	pha002888	1.77E-05	phs000272	1.28	[1.15-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
12	120098409	rs7310266	T	C	rs7310266	pha002888	5.81E-05	phs000272	1.28	[1.14-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
13	44457925	rs3764147	A	G	rs3764147	23291587	8.55E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
13	44457925	rs3764147	A	G	rs3764147	pha002888	7.36E-06	phs000272	1.33	[1.18-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	LACC1	missense	NM_153218
13	44471317	rs2121037	C	T	rs2121037	pha002888	4.56E-05	phs000272	1.32	[1.16-1.52]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
13	44475398	rs1373904	A	G	rs1373904	23291587	7.78E-06	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
13	46620135	rs1041167	A	T	rs1041167	23291587	2.55E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
13	99876281	rs9513584	G	A	rs9513584	19442274	5.00E-04	Beh?et's disease(Eye disease absent)	NA	NA	152 Turkish cases; 170 Turkish controls	Turkish(322)	ALL(322)	MEA(322)	ALL(322)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, N.I.H., Extramural	Comparative Study	A
14	21195471	rs8023192	A	C	rs8023192	pha002888	9.44E-05	phs000272	1.26	[1.12-1.41]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
14	90305660	rs4900016	A	G	rs4900016	pha002888	3.53E-05	phs000272	1.34	[1.17-1.54]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	EFCAB11	intron	NM_145231
15	54127905	rs8040564	A	G	rs8040564	23291587	2.92E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
15	54129073	rs7165549	G	A	rs7165549	23291587	1.14E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
15	58100949	rs597804	G	A	rs597804	pha002888	5.59E-05	phs000272	1.28	[1.14-1.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
15	78510819	rs11072744	G	T	rs11072744	pha002888	7.62E-05	phs000272	1.34	[1.16-1.56]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	ACSBG1	intron	NM_015162
15	95235133	rs2199724	G	T	rs2199724	pha002888	2.59E-05	phs000272	1.28	[1.14-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
15	95237961	rs2046006	C	A	rs2046006	pha002888	9.03E-05	phs000272	1.26	[1.12-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
17	8565356	rs6503137	T	C	rs6503137	pha002888	8.24E-05	phs000272	1.36	[1.17-1.59]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	T	NA	NA	NA
17	8633310	rs1971773	C	T	rs1971773	pha002888	5.48E-05	phs000272	1.26	[1.13-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	CCDC42	UTR-3	NM_144681
17	70066502	rs1558748	T	C	rs1558748	pha002888	5.35E-05	phs000272	1.32	[1.15-1.49]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	A	NA	NA	NA
18	50235853	rs9952236	A	G	rs9952236	23291587	2.39E-05	NA	NA	NA	435 Turkish cases with uveitis; 780 Turkish cases without uveitis; 1,278 Turkish controls	Turkish(2493)	ALL(2493)	MEA(2493)	ALL(2493)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Meta-Analysis	Research Support, Non-U.S. Gov't	Research Support, N.I.H., Intramural
19	35660450	rs2285515	T	C	rs2285515	pha002888	7.66E-05	phs000272	1.27	[1.12-1.43]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	FXYD5	intron	NM_144779
20	8074116	rs4239774	G	A	rs4239774	23041938	0.00000207	NA	NA	NA	367 Korean ancestry cases; 800 Korean ancestry controls	Korean(1167)	ALL(1167)	ASN(1167)	ALL(1167)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	Research Support, Non-U.S. Gov't	A	NA
20	48955424	rs913678	T	C	rs913678	pha002888	3.19E-05	phs000272	1.27	[1.13-1.42]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA
22	35581399	rs2187961	G	A	rs2187961	pha002888	7.84E-06	phs000272	2.63	[1.69-4.17]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	G	NA	NA	NA
22	35631544	rs2092331	C	T	rs2092331	pha002888	2.28E-05	phs000272	2.33	[1.56-3.45]	NA	ALL(0)	ALL(0)	Behcet's disease	HPOID:0011955	Hepatic granulomatosis	DOID:13241	Behcet's disease	D001528	Behcet Syndrome	EFOID:0003780	Behcet's disease	Behcet syndrome	NA	NA	C	NA	NA	NA

Mapped by lexical matching(Total Items:0)
(Waiting for update.)

Mapped by homologous gene(Total Items:0)
(Waiting for update.)

Chemical(Total Drugs:7)
CUI	ChemicalName	ChemicalID	CasRN	DiseaseName	DiseaseID	DirectEvidence	PubMedIDs
C0004943	chlorambucil	D002699	305-03-3	behcet syndrome	MESH:D001528	therapeutic	4796513
C0004943	colchicine	D003078	64-86-8	behcet syndrome	MESH:D001528	therapeutic	11087798
C0004943	cyclophosphamide	D003520	50-18-0	behcet syndrome	MESH:D001528	therapeutic	6788612
C0004943	cyclosporine	D016572	59865-13-3	behcet syndrome	MESH:D001528	therapeutic	11087798
C0004943	hydroxyurea	D006918	127-07-1	behcet syndrome	MESH:D001528	marker/mechanism	11426495
C0004943	tacrolimus	D016559	109581-93-3	behcet syndrome	MESH:D001528	therapeutic	7517134
C0004943	thalidomide	D013792	50-35-1	behcet syndrome	MESH:D001528	therapeutic	17852637

FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)

FDA labeling changes(Total Drugs:0)
(Waiting for update.)