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	atrial fibrillation

Disease ID	1197
Disease	atrial fibrillation
Definition	Abnormal cardiac rhythm that is characterized by rapid, uncoordinated firing of electrical impulses in the upper chambers of the heart (HEART ATRIA). In such case, blood cannot be effectively pumped into the lower chambers of the heart (HEART VENTRICLES). It is caused by abnormal impulse generation.
Synonym	af - atrial fibrillation afib atrial fibrillation (af) atrial fibrillation (disorder) atrial fibrillation [disease/finding] atrial fibrillations auricular fibrillation auricular fibrillations fibrillation - atrial fibrillation atrial fibrillation, atrial fibrillation, auricular fibrillations, atrial fibrillations, auricular
DOID	DOID:0060224
UMLS	C0004238
MeSH	D001281
SNOMED-CT	SNOMEDCT_US_2016_09_01:49436004
Comorbidity	UMLS \| Disease \| Sentences' Count(Total Sentences:201) C0018801 \| heart failure \| 136 C0040053 \| thrombus \| 55 C0027051 \| myocardial infarction \| 49 C0027051 \| myocardial infarct \| 49 C0018799 \| heart disease \| 48 C0155626 \| acute myocardial infarction \| 33 C0020538 \| hypertension \| 29 C0011847 \| diabetes \| 24 C0007194 \| hypertrophic cardiomyopathy \| 24 C0010068 \| coronary artery disease \| 21 C0878544 \| cardiomyopathy \| 17 C0022661 \| chronic kidney disease \| 16 C0007787 \| transient ischemic attack \| 15 C0011849 \| diabetes mellitus \| 15 C0022658 \| kidney disease \| 15 C0026265 \| mitral valve disease \| 14 C0011860 \| type 2 diabetes \| 13 C0026269 \| mitral stenosis \| 13 C0087086 \| thrombi \| 13 C0020550 \| hyperthyroidism \| 12 C0037315 \| sleep apnea \| 12 C0018802 \| congestive heart failure \| 12 C0042373 \| vascular disease \| 12 C0007785 \| cerebral infarct \| 12 C0022661 \| end-stage renal disease \| 11 C0520679 \| obstructive sleep apnea \| 10 C0040053 \| thrombosis \| 10 C0035439 \| rheumatic heart disease \| 10 C0011570 \| depression \| 10 C0022658 \| renal disease \| 10 C0007785 \| cerebral infarction \| 10 C0043202 \| wolff-parkinson-white syndrome \| 8 C0018824 \| valvular heart disease \| 8 C0028754 \| obesity \| 8 C0022116 \| ischemia \| 8 C0003507 \| aortic stenosis \| 7 C0007222 \| cardiovascular disease \| 7 C0037052 \| sick sinus syndrome \| 7 C1561644 \| chronic kidney disease (ckd) \| 6 C0948265 \| metabolic syndrome \| 6 C0264766 \| rheumatic mitral stenosis \| 6 C0024115 \| pulmonary disease \| 6 C0007785 \| cerebral ischemia \| 6 C0600260 \| obstructive pulmonary disease \| 6 C0007787 \| transient ischaemic attack \| 6 C0026266 \| mitral regurgitation \| 6 C0010068 \| coronary heart disease \| 5 C0006384 \| bundle branch block \| 5 C0033860 \| psoriasis \| 5 C0024117 \| chronic obstructive pulmonary disease \| 5 C0085580 \| essential hypertension \| 4 C0020542 \| pulmonary hypertension \| 4 C0018213 \| graves' disease \| 4 C0003873 \| rheumatoid arthritis \| 4 C0264716 \| chronic heart failure \| 4 C1135191 \| systolic heart failure \| 4 C0497327 \| dementia \| 4 C0027051 \| myocardial infarction (mi) \| 4 C0011860 \| type 2 diabetes mellitus \| 4 C0007787 \| transient ischemic attack (tia) \| 3 C0002726 \| amyloidosis \| 3 C1142166 \| brugada syndrome \| 3 C0017168 \| oesophageal reflux \| 3 C0242350 \| erectile dysfunction \| 3 C0017168 \| gastroesophageal reflux \| 3 C0017168 \| esophageal reflux disease \| 3 C0037315 \| sleep-disordered breathing \| 3 C0745140 \| hyperthyroid \| 3 C0014544 \| epileptic seizures \| 3 C0014544 \| epileptic seizure \| 3 C0022661 \| chronic renal failure \| 3 C0035078 \| renal failure \| 3 C0520679 \| obstructive sleep apnoea \| 3 C0037315 \| sleep apnoea \| 3 C0017168 \| esophageal reflux \| 3 C0003467 \| anxiety \| 3 C0017168 \| gastroesophageal reflux disease \| 3 C0020676 \| hypothyroidism \| 3 C0004245 \| atrioventricular block \| 3 C0007193 \| dilated cardiomyopathy \| 3 C0007785 \| cerebral infarctions \| 2 C0003864 \| arthritis \| 2 C0031039 \| pericardial effusion \| 2 C0007102 \| colon cancer \| 2 C0024115 \| lung disease \| 2 C0034065 \| pulmonary embolism \| 2 C0040127 \| thyroid storm \| 2 C0004153 \| atherosclerosis \| 2 C0022116 \| ischaemia \| 2 C0033687 \| proteinuria \| 2 C0010068 \| coronary disease \| 2 C0019069 \| hemophilia \| 2 C0026266 \| mitral valve regurgitation \| 2 C0152021 \| congenital heart disease \| 2 C0020538 \| high blood pressure \| 2 C0018799 \| cardiac disease \| 2 C0026265 \| mitral valvular disease \| 2 C0003507 \| aortic valve stenosis \| 2 C0852949 \| arterial disease \| 1 C0019069 \| haemophilia \| 1 C0398623 \| hypercoagulability state \| 1 C1704436 \| peripheral arterial disease \| 1 C0018801 \| cardiac failure \| 1 C0007570 \| coeliac disease \| 1 C0004943 \| behcet's disease \| 1 C0036202 \| sarcoidosis \| 1 C0030305 \| pancreatitis \| 1 C0398623 \| hypercoagulability \| 1 C0007222 \| cardiovascular diseases \| 1 C0520680 \| central sleep apnea \| 1 C0024299 \| lymphoma \| 1 C0037998 \| splenic infarction \| 1 C0029456 \| osteoporosis \| 1 C0040137 \| thyroid nodules \| 1 C0030920 \| peptic ulcer \| 1 C0003125 \| anorexia nervosa \| 1 C0014544 \| epilepsy \| 1 C0035309 \| retinal disease \| 1 C1332850 \| primary cardiac lymphoma \| 1 C0023895 \| hepatopathy \| 1 C0035309 \| retinal diseases \| 1 C1135196 \| diastolic heart failure \| 1 C0007787 \| transient ischaemic attacks \| 1 C0151744 \| myocardial ischemia \| 1 C0242379 \| lung cancer \| 1 C0035258 \| restless legs \| 1 C0002395 \| alzheimer's disease \| 1 C0022661 \| end-stage renal failure \| 1 C0026764 \| myeloma \| 1 C0011860 \| non-insulin dependent diabetes \| 1 C0018799 \| cardiac disorders \| 1 C0032285 \| pneumonia \| 1 C0751955 \| brain infarct \| 1 C0018824 \| heart valve diseases \| 1 C0878544 \| cardiomyopathies \| 1 C0264765 \| mitral valve diseases \| 1 C0007196 \| restrictive cardiomyopathy \| 1 C0042373 \| vascular diseases \| 1 C0018824 \| heart valve disease \| 1 C0035258 \| restless legs syndrome \| 1 C0023364 \| leptospirosis \| 1 C0003500 \| subvalvular aortic stenosis \| 1 C0024115 \| lung diseases \| 1 C0029463 \| osteosarcoma \| 1 C0026764 \| multiple myeloma \| 1 C0085615 \| right bundle branch block \| 1 C0002895 \| sickle cell disease \| 1 C0016522 \| patent foramen ovale \| 1 C0007930 \| chagas cardiomyopathy \| 1 C1565489 \| renal insufficiency \| 1 C0003537 \| aphasia \| 1 C0009402 \| colorectal cancer \| 1 C0009241 \| cognitive disorders \| 1 C0022661 \| end-stage kidney disease \| 1 C0018799 \| heart diseases \| 1 C0751955 \| brain infarction \| 1 C0011860 \| diabetes mellitus type 2 \| 1 C0020538 \| hypertensive disease \| 1 C0007785 \| cerebral infarcts \| 1 C0026848 \| myopathy \| 1 C0011854 \| insulin dependent diabetes \| 1 C0040156 \| thyrotoxicosis \| 1 C0020456 \| hyperglycemia \| 1 C0007570 \| celiac disease \| 1 C0023976 \| long qt syndrome \| 1 C1631597 \| catecholaminergic polymorphic ventricular tachycardia \| 1 C0152105 \| hypertensive heart disease \| 1 C0018802 \| congestive cardiac failure \| 1 C0151744 \| ischaemic heart disease \| 1 C0014118 \| endocarditis \| 1 C0022660 \| acute renal failure \| 1 C0026266 \| mitral insufficiency \| 1 C0026850 \| muscular dystrophy \| 1 C0282193 \| iron overload \| 1 C0162429 \| undernourished \| 1 C0040961 \| tricuspid regurgitation \| 1 C0011269 \| vascular dementia \| 1 C0040034 \| thrombocytopenia \| 1 C0917713 \| becker muscular dystrophy \| 1 C0007113 \| rectal cancer \| 1 C0007177 \| cardiac tamponade \| 1 C0268407 \| cardiac amyloidosis \| 1 C0040137 \| thyroid nodule \| 1 C0009319 \| colitis \| 1 C0029408 \| osteoarthritis \| 1 C0001339 \| acute pancreatitis \| 1 C0009324 \| ulcerative colitis \| 1 C0022661 \| end stage renal disease \| 1 C0019158 \| hepatitis \| 1 C0020456 \| hyperglycaemia \| 1 C0020676 \| hypothyroid \| 1 C0039538 \| teratoma \| 1 C0014038 \| encephalitis \| 1 C0031046 \| pericarditis \| 1 C0043202 \| wolff parkinson white syndrome \| 1 C0036421 \| systemic sclerosis \| 1 C0019204 \| hepatocellular carcinoma \| 1 C0003507 \| valvular aortic stenosis \| 1 C0043202 \| wolf-parkinson-white syndrome \| 1 C0392077 \| cardiac sarcoidosis \| 1 C0014121 \| bacterial endocarditis \| 1
Curated Gene	Entrez_id \| Symbol \| Resource(Total Genes:37) 4878 \| NPPA \| UniProtKB-KW 3784 \| KCNQ1 \| UniProtKB-KW;GHR 6324 \| SCN1B \| UniProtKB-KW 6910 \| TBX5 \| UniProtKB-KW 4524 \| MTHFR \| GWASCAT 6401 \| SELE \| CTD_human 1482 \| NKX2-5 \| CTD_human 5396 \| PRRX1 \| CTD_human 4846 \| NOS3 \| CTD_human 1674 \| DES \| CTD_human 10021 \| HCN4 \| CTD_human;GWASCAT 1636 \| ACE \| CTD_human 23224 \| SYNE2 \| CTD_human;GWASCAT 857 \| CAV1 \| CTD_human;GWASCAT 858 \| CAV2 \| CTD_human 4879 \| NPPB \| CTD_human 6331 \| SCN5A \| CLINVAR;CTD_human;UniProtKB-KW 6330 \| SCN4B \| UniProtKB-KW 1906 \| EDN1 \| CTD_human 7478 \| WNT8A \| CTD_human;GWASCAT 3759 \| KCNJ2 \| CLINVAR;UniProtKB-KW;GHR 3782 \| KCNN3 \| CTD_human;GWASCAT 6336 \| SCN10A \| CTD_human 10060 \| ABCC9 \| UniProtKB-KW 6327 \| SCN2B \| UniProtKB-KW 9992 \| KCNE2 \| CTD_human;UniProtKB-KW;GHR 2702 \| GJA5 \| UniProtKB-KW 3360 \| HTR4 \| CTD_human 2100 \| ESR2 \| GWASCAT 6660 \| SOX5 \| CTD_human 9631 \| NUP155 \| UniProtKB-KW 4635 \| MYL4 \| UniProtKB-KW 463 \| ZFHX3 \| CTD_human;GWASCAT 7450 \| VWF \| CTD_human 3741 \| KCNA5 \| CTD_human;UniProtKB-KW 84909 \| C9orf3 \| CTD_human;GWASCAT 55800 \| SCN3B \| UniProtKB-KW
Inferring Gene	Entrez_id \| Symbol \| Resource(Total Genes:66) 1636 \| ACE \| CIPHER;CTD_human 153 \| ADRB1 \| CIPHER 183 \| AGT \| CIPHER 185 \| AGTR1 \| CIPHER 54796 \| BNC2 \| CIPHER 4345 \| CD200 \| CIPHER 1071 \| CETP \| CIPHER 53942 \| CNTN5 \| CIPHER 1401 \| CRP \| CIPHER 1585 \| CYP11B2 \| CIPHER 1559 \| CYP2C9 \| CIPHER 1565 \| CYP2D6 \| CIPHER 4189 \| DNAJB9 \| CIPHER 1848 \| DUSP6 \| CIPHER 2099 \| ESR1 \| CIPHER 2162 \| F13A1 \| CIPHER 2702 \| GJA5 \| CIPHER 2784 \| GNB3 \| CIPHER 83872 \| HMCN1 \| CIPHER 3586 \| IL10 \| CIPHER 3741 \| KCNA5 \| CIPHER;CTD_human 3753 \| KCNE1 \| CIPHER 23704 \| KCNE4 \| CIPHER 3757 \| KCNH2 \| CIPHER 3762 \| KCNJ5 \| CIPHER 3782 \| KCNN3 \| CIPHER;CTD_human 3784 \| KCNQ1 \| CIPHER 220416 \| LRRC63 \| CIPHER 50488 \| MINK1 \| CIPHER 4313 \| MMP2 \| CIPHER 4524 \| MTHFR \| CIPHER 4846 \| NOS3 \| CIPHER;CTD_human 4878 \| NPPA \| CIPHER 5099 \| PCDH7 \| CIPHER 5308 \| PITX2 \| CIPHER 54715 \| RBFOX1 \| CIPHER 100271279 \| RPL13AP15 \| CIPHER 728010 \| RPL35P3 \| CIPHER 6176 \| RPLP1 \| CIPHER 55800 \| SCN3B \| CIPHER 6331 \| SCN5A \| CIPHER;CTD_human 9723 \| SEMA3E \| CIPHER 92369 \| SPSB4 \| CIPHER 55959 \| SULF2 \| CIPHER 6938 \| TCF12 \| CIPHER 8615 \| USO1 \| CIPHER 139538 \| VENTXP1 \| CIPHER 79001 \| VKORC1 \| CIPHER 463 \| ZFHX3 \| CIPHER;CTD_human 1482 \| NKX2-5 \| CTD_human 5396 \| PRRX1 \| CTD_human 857 \| CAV1 \| CTD_human 858 \| CAV2 \| CTD_human 23224 \| SYNE2 \| CTD_human 1906 \| EDN1 \| CTD_human 7478 \| WNT8A \| CTD_human 4879 \| NPPB \| CTD_human 1674 \| DES \| CTD_human 6401 \| SELE \| CTD_human 7450 \| VWF \| CTD_human 3360 \| HTR4 \| CTD_human 6660 \| SOX5 \| CTD_human 84909 \| C9orf3 \| CTD_human 10021 \| HCN4 \| CTD_human 9992 \| KCNE2 \| CTD_human 6336 \| SCN10A \| CTD_human
Text Mined Gene	Entrez_id \| Symbol \| Score \| Resource(Total Genes:259) 51205 \| ACP6 \| 1.394 \| DISEASES 51703 \| ACSL5 \| 2.967 \| DISEASES 88 \| ACTN2 \| 1.418 \| DISEASES 101 \| ADAM8 \| 2.112 \| DISEASES 11093 \| ADAMTS13 \| 1.222 \| DISEASES 116 \| ADCYAP1 \| 1.459 \| DISEASES 9370 \| ADIPOQ \| 2.083 \| DISEASES 84890 \| ADO \| 1.318 \| DISEASES 153 \| ADRB1 \| 3.482 \| DISEASES 155 \| ADRB3 \| 1.351 \| DISEASES 60312 \| AFAP1 \| 1.559 \| DISEASES 4299 \| AFF1 \| 1.12 \| DISEASES 183 \| AGT \| 2.154 \| DISEASES 186 \| AGTR2 \| 1.834 \| DISEASES 262 \| AMD1 \| 1.736 \| DISEASES 287 \| ANK2 \| 2.817 \| DISEASES 27063 \| ANKRD1 \| 1.319 \| DISEASES 26084 \| ARHGEF26 \| 1.207 \| DISEASES 10092 \| ARPC5 \| 1.298 \| DISEASES 415 \| ARSE \| 1.428 \| DISEASES 116969 \| ART5 \| 1.368 \| DISEASES 11016 \| ATF7 \| 3.084 \| DISEASES 488 \| ATP2A2 \| 2.752 \| DISEASES 27032 \| ATP2C1 \| 1.228 \| DISEASES 496 \| ATP4B \| 1.119 \| DISEASES 55845 \| BRK1 \| 1.043 \| DISEASES 64115 \| C10orf54 \| 1.52 \| DISEASES 149466 \| C1orf210 \| 1.181 \| DISEASES 84909 \| C9orf3 \| 2.959 \| DISEASES 765 \| CA6 \| 1.473 \| DISEASES 79886 \| CAAP1 \| 1.95 \| DISEASES 782 \| CACNB1 \| 1.209 \| DISEASES 799 \| CALCR \| 1.817 \| DISEASES 801 \| CALM1 \| 2.019 \| DISEASES 813 \| CALU \| 1.317 \| DISEASES 23066 \| CAND2 \| 1.954 \| DISEASES 84290 \| CAPNS2 \| 2.249 \| DISEASES 831 \| CAST \| 1.383 \| DISEASES 857 \| CAV1 \| 2.236 \| DISEASES 875 \| CBS \| 1.883 \| DISEASES 911 \| CD1C \| 2.017 \| DISEASES 959 \| CD40LG \| 2.043 \| DISEASES 9859 \| CEP170 \| 1.464 \| DISEASES 387119 \| CEP85L \| 1.357 \| DISEASES 1103 \| CHAT \| 2.009 \| DISEASES 1111 \| CHEK1 \| 1.327 \| DISEASES 1193 \| CLIC2 \| 1.109 \| DISEASES 1268 \| CNR1 \| 1.479 \| DISEASES 1269 \| CNR2 \| 2.092 \| DISEASES 22796 \| COG2 \| 1.016 \| DISEASES 1385 \| CREB1 \| 1.202 \| DISEASES 1471 \| CST3 \| 2.67 \| DISEASES 1490 \| CTGF \| 3.017 \| DISEASES 11330 \| CTRC \| 1.182 \| DISEASES 57703 \| CWC22 \| 3.025 \| DISEASES 1536 \| CYBB \| 2.781 \| DISEASES 1585 \| CYP11B2 \| 2.825 \| DISEASES 1557 \| CYP2C19 \| 1.576 \| DISEASES 1565 \| CYP2D6 \| 2.178 \| DISEASES 1573 \| CYP2J2 \| 1.547 \| DISEASES 1576 \| CYP3A4 \| 2.832 \| DISEASES 23564 \| DDAH2 \| 2.358 \| DISEASES 147409 \| DSG4 \| 1.564 \| DISEASES 50506 \| DUOX2 \| 2.363 \| DISEASES 1906 \| EDN1 \| 2.633 \| DISEASES 2010 \| EMD \| 2.243 \| DISEASES 2058 \| EPRS \| 1.687 \| DISEASES 54586 \| EQTN \| 3.053 \| DISEASES 3266 \| ERAS \| 1.812 \| DISEASES 2117 \| ETV3 \| 2.689 \| DISEASES 2159 \| F10 \| 4.516 \| DISEASES 2160 \| F11 \| 1.331 \| DISEASES 2149 \| F2R \| 1.55 \| DISEASES 2152 \| F3 \| 4.803 \| DISEASES 2155 \| F7 \| 3.083 \| DISEASES 2157 \| F8 \| 1.406 \| DISEASES 2170 \| FABP3 \| 1.663 \| DISEASES 11124 \| FAF1 \| 1.365 \| DISEASES 100302740 \| FAS-AS1 \| 3.438 \| DISEASES 2192 \| FBLN1 \| 1.436 \| DISEASES 201456 \| FBXO15 \| 1.485 \| DISEASES 11153 \| FICD \| 1.908 \| DISEASES 2281 \| FKBP1B \| 3.04 \| DISEASES 2316 \| FLNA \| 1.298 \| DISEASES 2326 \| FMO1 \| 1.497 \| DISEASES 2335 \| FN1 \| 1.753 \| DISEASES 22862 \| FNDC3A \| 1.109 \| DISEASES 4303 \| FOXO4 \| 2.402 \| DISEASES 22844 \| FRMPD1 \| 1.61 \| DISEASES 2596 \| GAP43 \| 3.215 \| DISEASES 2626 \| GATA4 \| 2.002 \| DISEASES 10052 \| GJC1 \| 3.896 \| DISEASES 23426 \| GRIP1 \| 1.397 \| DISEASES 2869 \| GRK5 \| 1.335 \| DISEASES 9464 \| HAND2 \| 1.509 \| DISEASES 3043 \| HBB \| 1.258 \| DISEASES 3055 \| HCK \| 3.946 \| DISEASES 9734 \| HDAC9 \| 1.069 \| DISEASES 23493 \| HEY2 \| 1.305 \| DISEASES 3142 \| HLX \| 1.478 \| DISEASES 84525 \| HOPX \| 1.487 \| DISEASES 3303 \| HSPA1A \| 1.752 \| DISEASES 3316 \| HSPB2 \| 2.081 \| DISEASES 3329 \| HSPD1 \| 1.293 \| DISEASES 3347 \| HTN3 \| 1.139 \| DISEASES 3360 \| HTR4 \| 2.773 \| DISEASES 3363 \| HTR7 \| 1.4 \| DISEASES 3376 \| IARS \| 2.551 \| DISEASES 3586 \| IL10 \| 2.189 \| DISEASES 133396 \| IL31RA \| 1.873 \| DISEASES 259307 \| IL4I1 \| 3.316 \| DISEASES 3570 \| IL6R \| 1.64 \| DISEASES 51147 \| ING4 \| 1.658 \| DISEASES 154865 \| IQUB \| 2.171 \| DISEASES 729920 \| ISPD \| 1.251 \| DISEASES 3709 \| ITPR2 \| 1.249 \| DISEASES 3710 \| ITPR3 \| 2.438 \| DISEASES 57158 \| JPH2 \| 1.535 \| DISEASES 102723508 \| KANTR \| 2.971 \| DISEASES 3736 \| KCNA1 \| 1.154 \| DISEASES 3739 \| KCNA4 \| 3.307 \| DISEASES 7881 \| KCNAB1 \| 1.764 \| DISEASES 8514 \| KCNAB2 \| 1.73 \| DISEASES 3745 \| KCNB1 \| 1.52 \| DISEASES 9312 \| KCNB2 \| 1.051 \| DISEASES 3751 \| KCND2 \| 3.512 \| DISEASES 3753 \| KCNE1 \| 4.643 \| DISEASES 30820 \| KCNIP1 \| 1.011 \| DISEASES 30819 \| KCNIP2 \| 3.693 \| DISEASES 3767 \| KCNJ11 \| 1.787 \| DISEASES 3768 \| KCNJ12 \| 2.13 \| DISEASES 3762 \| KCNJ5 \| 4.186 \| DISEASES 3775 \| KCNK1 \| 2.572 \| DISEASES 89822 \| KCNK17 \| 1.027 \| DISEASES 3776 \| KCNK2 \| 3.17 \| DISEASES 50801 \| KCNK4 \| 2.39 \| DISEASES 51520 \| LARS \| 1.198 \| DISEASES 378805 \| LINC-PINT \| 1.031 \| DISEASES 4000 \| LMNA \| 2.123 \| DISEASES 57692 \| MAGEE1 \| 1.103 \| DISEASES 4151 \| MB \| 2.386 \| DISEASES 51562 \| MBIP \| 1.548 \| DISEASES 8972 \| MGAM \| 2.7 \| DISEASES 84709 \| MGARP \| 1.417 \| DISEASES 104564225 \| MHRT \| 3.46 \| DISEASES 50488 \| MINK1 \| 1.052 \| DISEASES 4311 \| MME \| 1.083 \| DISEASES 4312 \| MMP1 \| 2.537 \| DISEASES 4318 \| MMP9 \| 2.743 \| DISEASES 4514 \| MT-CO3 \| 1.652 \| DISEASES 22823 \| MTF2 \| 1.012 \| DISEASES 4524 \| MTHFR \| 1.72 \| DISEASES 347273 \| MURC \| 2.124 \| DISEASES 4607 \| MYBPC3 \| 2.12 \| DISEASES 23077 \| MYCBP2 \| 1.079 \| DISEASES 4624 \| MYH6 \| 1.241 \| DISEASES 4625 \| MYH7 \| 2.388 \| DISEASES 4635 \| MYL4 \| 2.7 \| DISEASES 85366 \| MYLK2 \| 1.054 \| DISEASES 58529 \| MYOZ1 \| 3.107 \| DISEASES 10004 \| NAALADL1 \| 1.07 \| DISEASES 89796 \| NAV1 \| 2.972 \| DISEASES 4686 \| NCBP1 \| 1.329 \| DISEASES 4689 \| NCF4 \| 1.473 \| DISEASES 4771 \| NF2 \| 1.074 \| DISEASES 4776 \| NFATC4 \| 1.789 \| DISEASES 4774 \| NFIA \| 1.327 \| DISEASES 4803 \| NGF \| 1.791 \| DISEASES 1482 \| NKX2-5 \| 3.316 \| DISEASES 9722 \| NOS1AP \| 1.06 \| DISEASES 4878 \| NPPA \| 4.465 \| DISEASES 4879 \| NPPB \| 5.22 \| DISEASES 4881 \| NPR1 \| 1.701 \| DISEASES 4882 \| NPR2 \| 1.658 \| DISEASES 4306 \| NR3C2 \| 2.739 \| DISEASES 55301 \| OLAH \| 1.922 \| DISEASES 103752588 \| PACERR \| 3.901 \| DISEASES 89932 \| PAPLN \| 1.637 \| DISEASES 5144 \| PDE4D \| 1.326 \| DISEASES 5155 \| PDGFB \| 1.212 \| DISEASES 23481 \| PES1 \| 1.217 \| DISEASES 57649 \| PHF12 \| 1.12 \| DISEASES 5293 \| PIK3CD \| 3.911 \| DISEASES 9373 \| PLAA \| 2.321 \| DISEASES 10654 \| PMVK \| 1.629 \| DISEASES 5627 \| PROS1 \| 1.606 \| DISEASES 9536 \| PTGES \| 2.169 \| DISEASES 5817 \| PVR \| 8.108 \| DISEASES 5861 \| RAB1A \| 1.391 \| DISEASES 5999 \| RGS4 \| 2.299 \| DISEASES 9628 \| RGS6 \| 1.751 \| DISEASES 387 \| RHOA \| 1.227 \| DISEASES 6241 \| RRM2 \| 3.536 \| DISEASES 23212 \| RRS1 \| 1.91 \| DISEASES 6262 \| RYR2 \| 4.542 \| DISEASES 26278 \| SACS \| 2.11 \| DISEASES 389432 \| SAMD5 \| 1.517 \| DISEASES 142891 \| SAMD8 \| 1.722 \| DISEASES 23328 \| SASH1 \| 1.464 \| DISEASES 10590 \| SCGN \| 2.039 \| DISEASES 6336 \| SCN10A \| 2.677 \| DISEASES 6324 \| SCN1B \| 2.063 \| DISEASES 6330 \| SCN4B \| 2.685 \| DISEASES 6331 \| SCN5A \| 5.129 \| DISEASES 113675 \| SDSL \| 1.349 \| DISEASES 6401 \| SELE \| 2.303 \| DISEASES 462 \| SERPINC1 \| 4.506 \| DISEASES 5345 \| SERPINF2 \| 1.875 \| DISEASES 253970 \| SFTA3 \| 1.011 \| DISEASES 6474 \| SHOX2 \| 2.723 \| DISEASES 6510 \| SLC1A5 \| 1.486 \| DISEASES 9376 \| SLC22A8 \| 1.327 \| DISEASES 7779 \| SLC30A1 \| 1.696 \| DISEASES 285641 \| SLC36A3 \| 1.236 \| DISEASES 8671 \| SLC4A4 \| 1.631 \| DISEASES 9498 \| SLC4A8 \| 1.958 \| DISEASES 79811 \| SLTM \| 2.249 \| DISEASES 4088 \| SMAD3 \| 1.415 \| DISEASES 9304 \| SNORD22 \| 1.237 \| DISEASES 25826 \| SNORD82 \| 1.838 \| DISEASES 387104 \| SOGA3 \| 2.67 \| DISEASES 6660 \| SOX5 \| 2.068 \| DISEASES 10011 \| SRA1 \| 1.684 \| DISEASES 63826 \| SRR \| 1.14 \| DISEASES 23648 \| SSBP3 \| 1.246 \| DISEASES 6818 \| SULT1A3 \| 3.015 \| DISEASES 445329 \| SULT1A4 \| 3.04 \| DISEASES 23224 \| SYNE2 \| 1.771 \| DISEASES 79933 \| SYNPO2L \| 3.753 \| DISEASES 255928 \| SYT14 \| 1.654 \| DISEASES 26115 \| TANC2 \| 1.385 \| DISEASES 29110 \| TBK1 \| 1.327 \| DISEASES 80312 \| TET1 \| 1.694 \| DISEASES 7054 \| TH \| 2.586 \| DISEASES 7056 \| THBD \| 3.279 \| DISEASES 7068 \| THRB \| 2.245 \| DISEASES 84548 \| TMEM185A \| 1.003 \| DISEASES 7110 \| TMF1 \| 2.832 \| DISEASES 7124 \| TNF \| 2.365 \| DISEASES 7137 \| TNNI3 \| 4.471 \| DISEASES 51086 \| TNNI3K \| 1.924 \| DISEASES 7138 \| TNNT1 \| 3.59 \| DISEASES 7139 \| TNNT2 \| 3.409 \| DISEASES 1861 \| TOR1A \| 1.261 \| DISEASES 94241 \| TP53INP1 \| 1.677 \| DISEASES 7179 \| TPTE \| 1.78 \| DISEASES 90933 \| TRIM41 \| 1.648 \| DISEASES 7222 \| TRPC3 \| 1.7 \| DISEASES 7273 \| TTN \| 1.348 \| DISEASES 27229 \| TUBGCP4 \| 1.36 \| DISEASES 7422 \| VEGFA \| 1.416 \| DISEASES 79001 \| VKORC1 \| 5.411 \| DISEASES 23038 \| WDTC1 \| 2.676 \| DISEASES 7478 \| WNT8A \| 1.774 \| DISEASES 114786 \| XKR4 \| 1.413 \| DISEASES 339487 \| ZBTB8OS \| 1.642 \| DISEASES 80829 \| ZFP91 \| 1.111 \| DISEASES 7702 \| ZNF143 \| 4.529 \| DISEASES 149076 \| ZNF362 \| 1.407 \| DISEASES
Locus	(Waiting for update.)

Disease ID	1197
Disease	atrial fibrillation
Integrated Phenotype	(Waiting for update.)
Text Mined Phenotype	HPO \| Name \| Sentences' Count(Total Phenotypes:169) HP:0001297 \| Cerebral vascular events \| 866 HP:0001907 \| Thromboembolic disease \| 149 HP:0001635 \| Congestive heart failure \| 143 HP:0002140 \| Ischemic stroke \| 125 HP:0001658 \| Myocardial infarction \| 47 HP:0001649 \| Tachycardia \| 35 HP:0000822 \| Hypertension \| 33 HP:0011675 \| Arrhythmias \| 28 HP:0001639 \| Hypertrophic cardiomyopathy \| 25 HP:0002326 \| TIA \| 22 HP:0001677 \| Coronary artery disease \| 22 HP:0001638 \| Cardiomyopathy \| 19 HP:0012622 \| Chronic kidney disease \| 17 HP:0003774 \| End-stage renal failure \| 16 HP:0010535 \| Sleep apnea \| 15 HP:0002104 \| Absence of spontaneous respiration \| 15 HP:0000819 \| Diabetes mellitus \| 15 HP:0000836 \| Overactive thyroid \| 14 HP:0001718 \| Mitral stenosis \| 14 HP:0001662 \| Bradycardia \| 12 HP:0002870 \| Obstructive sleep apnea \| 11 HP:0000716 \| Depression \| 10 HP:0001650 \| Valvular aortic stenosis \| 9 HP:0001712 \| Left ventricular hypertrophy \| 9 HP:0002170 \| Intracranial hemorrhage \| 8 HP:0001653 \| Mitral valve insufficiency \| 8 HP:0001631 \| Atria septal defect \| 8 HP:0001513 \| Obesity \| 8 HP:0001727 \| Thromboembolic stroke \| 8 HP:0011704 \| Sick sinus syndrome \| 8 HP:0001716 \| Wolff-Parkinson-White syndrome \| 8 HP:0100543 \| Cognitive deficits \| 8 HP:0002584 \| Intestinal hemorrhage \| 7 HP:0001279 \| Syncope \| 7 HP:0004755 \| Supraventricular tachycardia \| 7 HP:0001714 \| Ventricular hypertrophy \| 7 HP:0004756 \| Ventricular tachycardia \| 7 HP:0002637 \| Brain ischemia \| 6 HP:0004757 \| Paroxysmal atrial fibrillation \| 6 HP:0011710 \| Bundle-branch block \| 6 HP:0004749 \| Atrial flutter \| 6 HP:0002239 \| Gastrointestinal hemorrhage \| 6 HP:0003765 \| Psoriasis \| 5 HP:0000821 \| Underactive thyroid \| 5 HP:0006510 \| Chronic obstructive pulmonary disease \| 5 HP:0000083 \| Renal insufficiency \| 4 HP:0011713 \| Left bundle branch block \| 4 HP:0001342 \| Intracerebral hemorrhage \| 4 HP:0002617 \| Aneurysmal dilatation \| 4 HP:0001268 \| Mental deterioration \| 4 HP:0001250 \| Seizures \| 4 HP:0000726 \| Dementia \| 4 HP:0002092 \| Pulmonary artery hypertension \| 4 HP:0002527 \| Falls \| 4 HP:0001962 \| Palpitations \| 4 HP:0001370 \| Rheumatoid arthritis \| 4 HP:0002615 \| Low blood pressure \| 3 HP:0000802 \| Erectile dysfunction \| 3 HP:0004763 \| Episodic supraventricular tachycardia \| 3 HP:0002204 \| Pulmonary embolism \| 3 HP:0002020 \| Heartburn \| 3 HP:0001698 \| Pericardial effusions \| 3 HP:0004309 \| Pre-excitation syndrome \| 3 HP:0001644 \| Congestive cardiomyopathy \| 3 HP:0011034 \| Amyloid disease \| 3 HP:0001678 \| Atrioventricular block \| 3 HP:0000739 \| Anxiety \| 3 HP:0001645 \| Sudden cardiac death \| 3 HP:0002094 \| Dyspnea \| 3 HP:0001369 \| Arthritis \| 3 HP:0100806 \| Sepsis \| 3 HP:0005162 \| Left ventricular impairment \| 2 HP:0001627 \| Congenital heart defects \| 2 HP:0004950 \| Peripheral artery disease \| 2 HP:0005301 \| Persistent left superior vena cava \| 2 HP:0003003 \| Colon cancer \| 2 HP:0001681 \| Angina pectoris \| 2 HP:0012668 \| Situational syncope \| 2 HP:0002315 \| Headaches \| 2 HP:0100584 \| Endocarditis \| 2 HP:0002625 \| Blood clot in a deep vein \| 2 HP:0100749 \| Thoracic pain \| 2 HP:0002621 \| Atherosclerosis \| 2 HP:0000093 \| Proteinuria \| 2 HP:0011877 \| Increased mean platelet volume \| 2 HP:0002647 \| Aortic dissection \| 2 HP:0011995 \| Atrial septal aneurysm \| 2 HP:0002459 \| Dysautonomia \| 2 HP:0001657 \| Prolonged QT interval \| 2 HP:0012248 \| Lengthened PR interval on EKG \| 1 HP:0004398 \| Peptic ulcer \| 1 HP:0001288 \| Gait disturbance \| 1 HP:0002608 \| Celiac disease \| 1 HP:0001682 \| Subvalvular aortic stenosis \| 1 HP:0002069 \| Generalized tonic clonic seizures \| 1 HP:0002758 \| Osteoarthritis \| 1 HP:0001917 \| Renal amyloidosis \| 1 HP:0006775 \| Multiple myeloma \| 1 HP:0002039 \| Anorexia \| 1 HP:0100598 \| Pulmonary oedema \| 1 HP:0100665 \| Angiooedema \| 1 HP:0000872 \| Hashimoto's thyroiditis \| 1 HP:0004308 \| Ventricular arrhythmia \| 1 HP:0002018 \| Nausea \| 1 HP:0004420 \| Arterial thrombosis \| 1 HP:0002583 \| Colitis \| 1 HP:0005180 \| Tricuspid insufficiency \| 1 HP:0011703 \| Sinus tach \| 1 HP:0005115 \| arrhythmias, Supraventricular \| 1 HP:0030843 \| Cardiac amyloidosis \| 1 HP:0007359 \| Partial seizures \| 1 HP:0001669 \| Transposition of the great arteries \| 1 HP:0001636 \| Tetrology of fallot \| 1 HP:0001919 \| Acute renal failure \| 1 HP:0001701 \| Pericarditis \| 1 HP:0002344 \| Progressive neurologic deterioration \| 1 HP:0002301 \| Hemiplegia \| 1 HP:0002669 \| Osteosarcoma \| 1 HP:0001663 \| Ventricular fibrillation \| 1 HP:0001651 \| Thoracic situs inversus \| 1 HP:0000767 \| Funnel chest \| 1 HP:0002153 \| Elevated serum potassium levels \| 1 HP:0002155 \| Increased triglycerides \| 1 HP:0002013 \| Emesis \| 1 HP:0001695 \| Cardiac arrest \| 1 HP:0002664 \| Neoplasia \| 1 HP:0012735 \| Coughing \| 1 HP:0001945 \| Fever \| 1 HP:0012377 \| Hemianopia \| 1 HP:0002189 \| Excessive daytime sleepiness \| 1 HP:0001262 \| Somnolence \| 1 HP:0002359 \| Frequent falls \| 1 HP:0100790 \| Hernia \| 1 HP:0011748 \| Adrenocorticotropic hormone deficiency \| 1 HP:0002665 \| Lymphoma \| 1 HP:0001873 \| Low platelet count \| 1 HP:0001402 \| Hepatocellular carcinoma \| 1 HP:0100279 \| Ulcerative colitis \| 1 HP:0100724 \| Hypercoagulability \| 1 HP:0005157 \| Concentric hypertrophic cardiomyopathy \| 1 HP:0002015 \| Swallowing difficulty \| 1 HP:0004936 \| Blood clot in vein \| 1 HP:0006554 \| Acute hepatic failure \| 1 HP:0000969 \| Dropsy \| 1 HP:0007430 \| Generalized edema \| 1 HP:0001733 \| Pancreatic inflammation \| 1 HP:0001735 \| Acute pancreatitis \| 1 HP:0010536 \| Central sleep apnoea \| 1 HP:0030741 \| Teratoma of the mediastinum \| 1 HP:0000832 \| Primary hypothyroidism \| 1 HP:0012531 \| Pain \| 1 HP:0012452 \| Restless legs \| 1 HP:0002381 \| Aphasia \| 1 HP:0000820 \| Thyroid abnormality \| 1 HP:0003074 \| High blood glucose \| 1 HP:0000939 \| Osteoporosis \| 1 HP:0011712 \| Right bundle-branch block \| 1 HP:0001824 \| Weight loss \| 1 HP:0003198 \| Myopathic changes \| 1 HP:0001655 \| Patent foramen ovale \| 1 HP:0009792 \| Teratoma \| 1 HP:0001399 \| Liver failure \| 1 HP:0002383 \| Encephalitis \| 1 HP:0001723 \| Restrictive cardiomyopathy \| 1 HP:0002090 \| Pneumonia \| 1 HP:0003560 \| Muscular dystrophy \| 1 HP:0012625 \| Stage 3 chronic kidney disease \| 1 HP:0012115 \| Liver inflammation \| 1 HP:0006528 \| Chronic lung disease \| 1

Disease ID	1197
Disease	atrial fibrillation
Manually Symptom	(Waiting for update.)
Text Mined Symptom	(Waiting for update.)

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

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

All Snps(Total Genotypes:46)
snpId	pubmedId	geneId	geneSymbol	diseaseId	sourceId	sentence	score	Year	geneSymbol_dbSNP	CHROMOSOME	POS	REF	ALT
rs10033464	17603472	5308	PITX2	umls:C0004238	GAD	[Variants conferring risk of atrial fibrillation on chromosome 4q25.]	0.01183516	2007	NA	4	110799605	T	G
rs10489717	17903304	83872	HMCN1	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	HMCN1	1	185954443	G	A
rs10492755	17903304	54715	RBFOX1	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	RBFOX1	16	7511457	C	T
rs10501920	17903304	53942	CNTN5	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	CNTN5	11	99622442	C	G
rs10511311	17903304	4345	CD200	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	CD200;SLC9C1	3	112336992	A	T
rs10821415	22544366	84909	C9orf3	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.24	2012	C9orf3	9	94951177	C	A
rs1152591	22544366	23224	SYNE2	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.24	2012	ESR2;SYNE2	14	64214130	A	G
rs1152591	22544366	2100	ESR2	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.12	2012	ESR2;SYNE2	14	64214130	A	G
rs11973337	17903304	9723	SEMA3E	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	NA	7	83662101	A	G
rs1298340	17903304	5890	RAD51B	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	RAD51B	14	68210775	G	C
rs13038095	20173747	55959	SULF2	umls:C0004238	GAD	[Common variants in KCNN3 are associated with lone atrial fibrillation.]	0.002367032	2010	NA	20	47796832	G	T
rs1314913	17903304	5890	RAD51B	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	RAD51B	14	68232877	C	T
rs13376333	20173747	3782	KCNN3	umls:C0004238	GWASCAT	Common variants in KCNN3 are associated with lone atrial fibrillation.	0.242367032	2010	KCNN3	1	154841877	C	T
rs13376333	20173747	3782	KCNN3	umls:C0004238	GAD	[Common variants in KCNN3 are associated with lone atrial fibrillation.]	0.242367032	2010	KCNN3	1	154841877	C	T
rs1427828	17903304	1848	DUSP6	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	LOC105369889	12	89368722	C	G
rs147750704	NA	3759	KCNJ2	umls:C0004238	CLINVAR	NA	0.12272435	NA	KCNJ2	17	70175316	G	A
rs1558145	17903304	139538	VENTXP1	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	NA	X	26637619	C	T
rs16851040	17903304	92369	SPSB4	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	SPSB4	3	141073523	A	G
rs17042171	19597492	5308	PITX2	umls:C0004238	GAD	[Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.]	0.01183516	2009	NA	4	110787131	C	A
rs17375901	19597492	4878	NPPA	umls:C0004238	GAD	[Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.]	0.005091382	2009	MTHFR	1	11792459	C	T
rs17375901	19597492	4524	MTHFR	umls:C0004238	GAD	[Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.]	0.122367032	2009	MTHFR	1	11792459	C	T
rs17375901	19597492	4524	MTHFR	umls:C0004238	GWASCAT	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.	0.122367032	2009	MTHFR	1	11792459	C	T
rs1751382	17903304	5890	RAD51B	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	RAD51B	14	68225933	C	T
rs199473060	NA	6331	SCN5A	umls:C0004238	CLINVAR	NA	0.262732561	NA	SCN5A	3	38622468	C	T
rs199473111	NA	6331	SCN5A	umls:C0004238	CLINVAR	NA	0.262732561	NA	SCN5A	3	38606007	C	T
rs199473260	NA	6331	SCN5A	umls:C0004238	CLINVAR	NA	0.262732561	NA	SCN5A	3	38555720	T	C
rs199473335	NA	6331	SCN5A	umls:C0004238	CLINVAR	NA	0.262732561	NA	SCN5A	3	38550411	G	T
rs2040862	22544366	7478	WNT8A	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.24	2012	WNT8A	5	138084300	C	T
rs2106261	22544366	463	ZFHX3	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.244734064	2012	ZFHX3	16	73017721	C	T
rs2106261	19597492	463	ZFHX3	umls:C0004238	GWASCAT	Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.	0.244734064	2009	ZFHX3	16	73017721	C	T
rs2106261	19597492	463	ZFHX3	umls:C0004238	GAD	[Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.]	0.244734064	2009	ZFHX3	16	73017721	C	T
rs2200733	17603472	5308	PITX2	umls:C0004238	GAD	[Variants conferring risk of atrial fibrillation on chromosome 4q25.]	0.01183516	2007	NA	4	110789013	C	T
rs2200733	19597491	5308	PITX2	umls:C0004238	GAD	[A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.]	0.01183516	2009	NA	4	110789013	C	T
rs2421954	17903304	51057	WDPCP	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	WDPCP	2	63527141	T	C
rs324735	17903304	8615	USO1	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	USO1	4	75783861	A	T
rs3807989	22544366	857	CAV1	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.24	2012	CAV1	7	116546187	A	G
rs412253	17903304	5099	PCDH7	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	NA	4	31441128	T	A
rs4776472	17903304	6176	RPLP1	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	NA	15	69714534	G	A
rs6666258	22544366	3782	KCNN3	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.242367032	2012	KCNN3	1	154841792	G	C
rs6843082	20173747	5308	PITX2	umls:C0004238	GAD	[Common variants in KCNN3 are associated with lone atrial fibrillation.]	0.01183516	2010	NA	4	110796911	G	A
rs7164883	22544366	10021	HCN4	umls:C0004238	GWASCAT	Meta-analysis identifies six new susceptibility loci for atrial fibrillation.	0.24	2012	HCN4	15	73359833	A	G
rs7193343	19597491	463	ZFHX3	umls:C0004238	GWASCAT	A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.	0.244734064	2009	ZFHX3	16	72995261	T	C
rs7193343	19597491	463	ZFHX3	umls:C0004238	GAD	[A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.]	0.244734064	2009	ZFHX3	16	72995261	T	C
rs7781585	17903304	4189	DNAJB9	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	NA	7	108824307	C	T
rs935329	17903304	6938	TCF12	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	TCF12	15	57217763	C	G
rs958546	17903304	220416	LRRC63	umls:C0004238	GAD	[No association attained genome-wide significance, but several intriguing findings emerged. Notably, we replicated associations of chromosome 9p21 with major CVD. Additional studies are needed to validate these results. Finding genetic variants associated ]	0.002367032	2007	LRRC63	13	46259582	G	C

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

GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)

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

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

Disease ID	1197
Disease	atrial fibrillation
Case	(Waiting for update.)