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Pediatric Disease Annotations & Medicines



   keratosis
  

Disease ID 1225
Disease keratosis
Definition
Any horny growth such as a wart or callus.
Synonym
keratoses
keratosis (disorder)
keratosis [disease/finding]
DOID
UMLS
C0022593
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:17)
C0007137  |  squamous cell carcinoma  |  4
C0020758  |  ichthyosis congenita  |  3
C0020757  |  ichthyosis  |  3
C0007117  |  basal cell carcinoma  |  3
C0014859  |  esophageal cancer  |  1
C0011603  |  dermatitis  |  1
C0812437  |  oculodentodigital dysplasia  |  1
C0002991  |  dermatofibroma  |  1
C0022596  |  palmoplantar keratoderma  |  1
C0023267  |  leiomyoma  |  1
C0013595  |  eczema  |  1
C0022602  |  actinic keratoses  |  1
C0031106  |  early-onset periodontitis  |  1
C0023646  |  lichen planus  |  1
C0007117  |  basal cell carcinomas  |  1
C0011615  |  atopic dermatitis  |  1
C0022572  |  keratoacanthoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:38)
TP53  |  7157  |  CTD_human
ATP2A2  |  488  |  GHR
KRT14  |  3861  |  UniProtKB-KW
KEAP1  |  9817  |  CTD_human
DSP  |  1832  |  UniProtKB-KW
CAST  |  831  |  UniProtKB-KW
GJB6  |  10804  |  UniProtKB-KW
NFE2L2  |  4780  |  CTD_human
CAT  |  847  |  CTD_human
JUP  |  3728  |  UniProtKB-KW
KRT16  |  3868  |  UniProtKB-KW
KRT17  |  3872  |  UniProtKB-KW
GJA1  |  2697  |  UniProtKB-KW
DSG1  |  1828  |  UniProtKB-KW
SLURP1  |  57152  |  UniProtKB-KW
TAT  |  6898  |  UniProtKB-KW
MPO  |  4353  |  CTD_human
MBTPS2  |  51360  |  UniProtKB-KW
KRT9  |  3857  |  UniProtKB-KW
KRT1  |  3848  |  UniProtKB-KW
AQP5  |  362  |  UniProtKB-KW
GJB2  |  2706  |  UniProtKB-KW
SNAP29  |  9342  |  UniProtKB-KW
AAGAB  |  79719  |  UniProtKB-KW
CTSC  |  1075  |  UniProtKB-KW
LOR  |  4014  |  UniProtKB-KW
POMP  |  51371  |  UniProtKB-KW
GJB3  |  2707  |  UniProtKB-KW
KANK2  |  25959  |  UniProtKB-KW
TRPV3  |  162514  |  UniProtKB-KW
WNT10A  |  80326  |  UniProtKB-KW
SERPINB7  |  8710  |  UniProtKB-KW
KRT6B  |  3854  |  UniProtKB-KW
KRT6A  |  3853  |  UniProtKB-KW
KRT6C  |  286887  |  UniProtKB-KW
RHBDF2  |  79651  |  UniProtKB-KW
RSPO1  |  284654  |  UniProtKB-KW
GJB4  |  127534  |  UniProtKB-KW
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:318)
27184  |  DISC2  |  DISEASES
1407  |  CRY1  |  DISEASES
1015  |  CDH17  |  DISEASES
84245  |  MRI1  |  DISEASES
5318  |  PKP2  |  DISEASES
43847  |  KLK14  |  DISEASES
3861  |  KRT14  |  DISEASES
4680  |  CEACAM6  |  DISEASES
7051  |  TGM1  |  DISEASES
80863  |  PRRT1  |  DISEASES
9342  |  SNAP29  |  DISEASES
4174  |  MCM5  |  DISEASES
22795  |  NID2  |  DISEASES
1511  |  CTSG  |  DISEASES
9517  |  SPTLC2  |  DISEASES
10278  |  EFS  |  DISEASES
343637  |  RSPO4  |  DISEASES
412  |  STS  |  DISEASES
7076  |  TIMP1  |  DISEASES
54  |  ACP5  |  DISEASES
4313  |  MMP2  |  DISEASES
79650  |  USB1  |  DISEASES
9333  |  TGM5  |  DISEASES
23581  |  CASP14  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
3082  |  HGF  |  DISEASES
9487  |  PIGL  |  DISEASES
8456  |  FOXN1  |  DISEASES
51056  |  LAP3  |  DISEASES
1075  |  CTSC  |  DISEASES
595  |  CCND1  |  DISEASES
9733  |  SART3  |  DISEASES
11108  |  PRDM4  |  DISEASES
4598  |  MVK  |  DISEASES
10094  |  ARPC3  |  DISEASES
50856  |  CLEC4A  |  DISEASES
1839  |  HBEGF  |  DISEASES
3003  |  GZMK  |  DISEASES
5948  |  RBP2  |  DISEASES
5947  |  RBP1  |  DISEASES
5657  |  PRTN3  |  DISEASES
1509  |  CTSD  |  DISEASES
4317  |  MMP8  |  DISEASES
63923  |  TNN  |  DISEASES
8600  |  TNFSF11  |  DISEASES
10804  |  GJB6  |  DISEASES
5266  |  PI3  |  DISEASES
5335  |  PLCG1  |  DISEASES
56269  |  IRGC  |  DISEASES
27076  |  LYPD3  |  DISEASES
667  |  DST  |  DISEASES
2069  |  EREG  |  DISEASES
57152  |  SLURP1  |  DISEASES
3860  |  KRT13  |  DISEASES
3857  |  KRT9  |  DISEASES
29997  |  GLTSCR2  |  DISEASES
968  |  CD68  |  DISEASES
15  |  AANAT  |  DISEASES
6299  |  SALL1  |  DISEASES
3859  |  KRT12  |  DISEASES
3852  |  KRT5  |  DISEASES
3848  |  KRT1  |  DISEASES
286887  |  KRT6C  |  DISEASES
3854  |  KRT6B  |  DISEASES
3958  |  LGALS3  |  DISEASES
84034  |  EMILIN2  |  DISEASES
10462  |  CLEC10A  |  DISEASES
84246  |  MED10  |  DISEASES
1830  |  DSG3  |  DISEASES
1828  |  DSG1  |  DISEASES
1823  |  DSC1  |  DISEASES
80326  |  WNT10A  |  DISEASES
3569  |  IL6  |  DISEASES
640  |  BLK  |  DISEASES
27177  |  IL36B  |  DISEASES
10850  |  CCL27  |  DISEASES
7097  |  TLR2  |  DISEASES
1829  |  DSG2  |  DISEASES
9663  |  LPIN2  |  DISEASES
642  |  BLMH  |  DISEASES
64211  |  LHX5  |  DISEASES
999  |  CDH1  |  DISEASES
79719  |  AAGAB  |  DISEASES
64285  |  RHBDF1  |  DISEASES
9914  |  ATP2C2  |  DISEASES
1770  |  DNAH9  |  DISEASES
7011  |  TEP1  |  DISEASES
8503  |  PIK3R3  |  DISEASES
1  |  A1BG  |  DISEASES
7299  |  TYR  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
1991  |  ELANE  |  DISEASES
9410  |  SNRNP40  |  DISEASES
5317  |  PKP1  |  DISEASES
5290  |  PIK3CA  |  DISEASES
1001  |  CDH3  |  DISEASES
1475  |  CSTA  |  DISEASES
2247  |  FGF2  |  DISEASES
192666  |  KRT24  |  DISEASES
6774  |  STAT3  |  DISEASES
3383  |  ICAM1  |  DISEASES
4171  |  MCM2  |  DISEASES
1950  |  EGF  |  DISEASES
256076  |  COL6A5  |  DISEASES
4060  |  LUM  |  DISEASES
2252  |  FGF7  |  DISEASES
7157  |  TP53  |  DISEASES
3858  |  KRT10  |  DISEASES
126410  |  CYP4F22  |  DISEASES
207  |  AKT1  |  DISEASES
1513  |  CTSK  |  DISEASES
26154  |  ABCA12  |  DISEASES
7220  |  TRPC1  |  DISEASES
100996939  |  PYURF  |  DISEASES
9180  |  OSMR  |  DISEASES
1956  |  EGFR  |  DISEASES
1807  |  DPYS  |  DISEASES
6768  |  ST14  |  DISEASES
27250  |  PDCD4  |  DISEASES
1824  |  DSC2  |  DISEASES
2697  |  GJA1  |  DISEASES
3087  |  HHEX  |  DISEASES
204219  |  CERS3  |  DISEASES
197258  |  FUK  |  DISEASES
2063  |  NR2F6  |  DISEASES
114757  |  CYGB  |  DISEASES
3856  |  KRT8  |  DISEASES
121214  |  SDR9C7  |  DISEASES
362  |  AQP5  |  DISEASES
6707  |  SPRR3  |  DISEASES
7039  |  TGFA  |  DISEASES
1293  |  COL6A3  |  DISEASES
3313  |  HSPA9  |  DISEASES
4982  |  TNFRSF11B  |  DISEASES
1672  |  DEFB1  |  DISEASES
7373  |  COL14A1  |  DISEASES
1381  |  CRABP1  |  DISEASES
26253  |  CLEC4E  |  DISEASES
4314  |  MMP3  |  DISEASES
1292  |  COL6A2  |  DISEASES
4597  |  MVD  |  DISEASES
2125  |  EVPL  |  DISEASES
332  |  BIRC5  |  DISEASES
3868  |  KRT16  |  DISEASES
3688  |  ITGB1  |  DISEASES
1673  |  DEFB4A  |  DISEASES
10421  |  CD2BP2  |  DISEASES
8403  |  SOX14  |  DISEASES
50515  |  CHST11  |  DISEASES
6699  |  SPRR1B  |  DISEASES
1473  |  CST5  |  DISEASES
160065  |  PATE1  |  DISEASES
121391  |  KRT74  |  DISEASES
54498  |  SMOX  |  DISEASES
4176  |  MCM7  |  DISEASES
3872  |  KRT17  |  DISEASES
5340  |  PLG  |  DISEASES
3964  |  LGALS8  |  DISEASES
3265  |  HRAS  |  DISEASES
3849  |  KRT2  |  DISEASES
3728  |  JUP  |  DISEASES
6578  |  SLCO2A1  |  DISEASES
1474  |  CST6  |  DISEASES
348938  |  NIPAL4  |  DISEASES
1240  |  CMKLR1  |  DISEASES
5319  |  PLA2G1B  |  DISEASES
59344  |  ALOXE3  |  DISEASES
242  |  ALOX12B  |  DISEASES
54434  |  SSH1  |  DISEASES
4026  |  LPP  |  DISEASES
79651  |  RHBDF2  |  DISEASES
4312  |  MMP1  |  DISEASES
153562  |  MARVELD2  |  DISEASES
5339  |  PLEC  |  DISEASES
29841  |  GRHL1  |  DISEASES
64332  |  NFKBIZ  |  DISEASES
349149  |  GJC3  |  DISEASES
23347  |  SMCHD1  |  DISEASES
26276  |  VPS33B  |  DISEASES
4166  |  CHST6  |  DISEASES
338324  |  S100A7A  |  DISEASES
3855  |  KRT7  |  DISEASES
9671  |  WSCD2  |  DISEASES
5367  |  PMCH  |  DISEASES
5332  |  PLCB4  |  DISEASES
23451  |  SF3B1  |  DISEASES
1174  |  AP1S1  |  DISEASES
8710  |  SERPINB7  |  DISEASES
3753  |  KCNE1  |  DISEASES
25818  |  KLK5  |  DISEASES
66004  |  LYNX1  |  DISEASES
3266  |  ERAS  |  DISEASES
5329  |  PLAUR  |  DISEASES
4889  |  NPY5R  |  DISEASES
84720  |  PIGO  |  DISEASES
2261  |  FGFR3  |  DISEASES
10249  |  GLYAT  |  DISEASES
26578  |  OSTF1  |  DISEASES
6590  |  SLPI  |  DISEASES
10161  |  LPAR6  |  DISEASES
1499  |  CTNNB1  |  DISEASES
387837  |  CLEC12B  |  DISEASES
121549  |  ASCL4  |  DISEASES
127534  |  GJB4  |  DISEASES
160364  |  CLEC12A  |  DISEASES
6898  |  TAT  |  DISEASES
54892  |  NCAPG2  |  DISEASES
8736  |  MYOM1  |  DISEASES
284654  |  RSPO1  |  DISEASES
5625  |  PRODH  |  DISEASES
26151  |  NAT9  |  DISEASES
7867  |  MAPKAPK3  |  DISEASES
9931  |  HELZ  |  DISEASES
137797  |  LYPD2  |  DISEASES
799  |  CALCR  |  DISEASES
147409  |  DSG4  |  DISEASES
11005  |  SPINK5  |  DISEASES
489  |  ATP2A3  |  DISEASES
1825  |  DSC3  |  DISEASES
58484  |  NLRC4  |  DISEASES
9953  |  HS3ST3B1  |  DISEASES
2475  |  MTOR  |  DISEASES
3880  |  KRT19  |  DISEASES
1291  |  COL6A1  |  DISEASES
9851  |  KIAA0753  |  DISEASES
59352  |  LGR6  |  DISEASES
10090  |  UST  |  DISEASES
23328  |  SASH1  |  DISEASES
1382  |  CRABP2  |  DISEASES
10654  |  PMVK  |  DISEASES
6278  |  S100A7  |  DISEASES
4014  |  LOR  |  DISEASES
3713  |  IVL  |  DISEASES
4184  |  SMCP  |  DISEASES
2312  |  FLG  |  DISEASES
7062  |  TCHH  |  DISEASES
8036  |  SHOC2  |  DISEASES
10285  |  SMNDC1  |  DISEASES
2316  |  FLNA  |  DISEASES
63910  |  SLC17A9  |  DISEASES
959  |  CD40LG  |  DISEASES
55970  |  GNG12  |  DISEASES
23421  |  ITGB3BP  |  DISEASES
4070  |  TACSTD2  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
4318  |  MMP9  |  DISEASES
2707  |  GJB3  |  DISEASES
7099  |  TLR4  |  DISEASES
1650  |  DDOST  |  DISEASES
9500  |  MAGED1  |  DISEASES
84930  |  MASTL  |  DISEASES
3397  |  ID1  |  DISEASES
1041  |  CDSN  |  DISEASES
80318  |  GKAP1  |  DISEASES
29914  |  UBIAD1  |  DISEASES
6520  |  SLC3A2  |  DISEASES
284348  |  LYPD5  |  DISEASES
4609  |  MYC  |  DISEASES
8573  |  CASK  |  DISEASES
8559  |  PRPF18  |  DISEASES
646480  |  FABP9  |  DISEASES
6303  |  SAT1  |  DISEASES
51360  |  MBTPS2  |  DISEASES
4799  |  NFX1  |  DISEASES
1832  |  DSP  |  DISEASES
3853  |  KRT6A  |  DISEASES
51371  |  POMP  |  DISEASES
55858  |  TMEM165  |  DISEASES
2315  |  MLANA  |  DISEASES
93978  |  CLEC6A  |  DISEASES
9875  |  URB1  |  DISEASES
2706  |  GJB2  |  DISEASES
131405  |  TRIM71  |  DISEASES
3875  |  KRT18  |  DISEASES
284217  |  LAMA1  |  DISEASES
8632  |  DNAH17  |  DISEASES
11202  |  KLK8  |  DISEASES
5650  |  KLK7  |  DISEASES
9244  |  CRLF1  |  DISEASES
6397  |  SEC14L1  |  DISEASES
27032  |  ATP2C1  |  DISEASES
285848  |  PNPLA1  |  DISEASES
27023  |  FOXB1  |  DISEASES
6161  |  RPL32  |  DISEASES
5609  |  MAP2K7  |  DISEASES
8450  |  CUL4B  |  DISEASES
6654  |  SOS1  |  DISEASES
11137  |  PWP1  |  DISEASES
2260  |  FGFR1  |  DISEASES
1029  |  CDKN2A  |  DISEASES
25959  |  KANK2  |  DISEASES
387836  |  CLEC2A  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
6349  |  CCL3L1  |  DISEASES
2263  |  FGFR2  |  DISEASES
283987  |  HID1  |  DISEASES
3831  |  KLC1  |  DISEASES
285381  |  DPH3  |  DISEASES
100289462  |  DEFB4B  |  DISEASES
5333  |  PLCD1  |  DISEASES
83695  |  RHNO1  |  DISEASES
488  |  ATP2A2  |  DISEASES
3851  |  KRT4  |  DISEASES
23601  |  CLEC5A  |  DISEASES
8742  |  TNFSF12  |  DISEASES
4065  |  LY75  |  DISEASES
3892  |  KRT86  |  DISEASES
54749  |  EPDR1  |  DISEASES
820  |  CAMP  |  DISEASES
162514  |  TRPV3  |  DISEASES
7716  |  VEZF1  |  DISEASES
100129528  |  MUC8  |  DISEASES
102723508  |  KANTR  |  DISEASES
79104  |  MEG8  |  DISEASES
Locus(Waiting for update.)
Disease ID 1225
Disease keratosis
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:20)
HP:0030731  |  Carcinoma  |  5
HP:0002860  |  Squamous cell carcinoma  |  4
HP:0002671  |  Basalioma  |  3
HP:0008064  |  Ichthyosis  |  3
HP:0030410  |  Sebaceous carcinoma  |  2
HP:0003764  |  Naevus  |  2
HP:0002664  |  Neoplasia  |  2
HP:0045075  |  Hypotrichosis of eyebrow  |  1
HP:0001036  |  Parakeratosis  |  1
HP:0010783  |  Erythema  |  1
HP:0001047  |  Atopic dermatitis  |  1
HP:0000995  |  Beauty mark  |  1
HP:0002224  |  Woolly hair  |  1
HP:0000964  |  Eczema  |  1
HP:0003077  |  Hyperlipidemia  |  1
HP:0000982  |  Palmoplantar keratoderma  |  1
HP:0100534  |  Episcleritis  |  1
HP:0200043  |  Verrucae  |  1
HP:0012531  |  Pain  |  1
HP:0000958  |  Xerosis  |  1
Disease ID 1225
Disease keratosis
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:2)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:19)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs105213317374727328APEX1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007OGG1;CAMK139757089CG
rs1052133173747277515XRCC1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007OGG1;CAMK139757089CG
rs1052133173747274968OGG1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007OGG1;CAMK139757089CG
rs113040917374727328APEX1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007APEX1;OSGEP1420456995TA,G
rs1130409173747274968OGG1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007APEX1;OSGEP1420456995TA,G
rs1130409173747277515XRCC1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007APEX1;OSGEP1420456995TA,G
rs11348802217159915673BRAFumls:C0022593BeFreeAssociations with the BRAF(T1799A) mutation (P<0.05) were as follows: low tumor thickness (odds ratio (OR)=3.3); low mitotic rate (OR=2.0); low Ki67 score (OR=5.0); low PH3 score (OR=3.3); superficial spreading melanoma (OR=10.0); pigmented melanoma (OR=3.7); a lack of history of solar keratoses (OR=2.7); a location on the trunk (OR=3.4) or extremity (OR=2.0); a high level of self-reported childhood sun exposure (OR=2.0); < or =50 years of age (OR=2.5); and fewer freckles (OR=2.5).0.0008143262007BRAF7140753336AT,G,C
rs1799782173747274968OGG1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007XRCC11943553422GA
rs179978217374727328APEX1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007XRCC11943553422GA
rs1799782173747277515XRCC1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007XRCC11943553422GA
rs2548717374727328APEX1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007XRCC11943551574TC
rs25487173747277515XRCC1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007XRCC11943551574TC
rs25487173747274968OGG1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007XRCC11943551574TC
rs386493716173747274968OGG1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007NANANANANA
rs38649371617374727328APEX1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007NANANANANA
rs386493716173747277515XRCC1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007NANANANANA
rs38654554617374727328APEX1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007NANANANANA
rs386545546173747274968OGG1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007NANANANANA
rs386545546173747277515XRCC1umls:C0022593BeFreeData from a case-control study of 792 cases and 792 matched controls conducted in Bangladesh from 2001 to 2003 were analyzed using conditional logistic regression to assess the associations between four common base excision repair (BER) genetic polymorphisms X-ray repair cross-complementing group 1 (XRCC1) Arg399Gln, XRCC1 Arg194Trp, human 8-oxoguanine DNA glycosylase (hOGG1) Ser326Cys and apurinic/apyrimidinic endonuclease (APE1) Asp148Glu and arsenic-induced skin lesions including melanosis and keratosis.0.0002714422007NANANANANA
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.)
Chemical(Total Drugs:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)