rs25487, XRCC1

N. diseases: 205
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2002 2002
Gastric Cardia Carcinoma
CUI: C1333763
Disease: Gastric Cardia Carcinoma
13 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2004 2004
Leukemogenesis
CUI: C0598766
Disease: Leukemogenesis
25 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2004 2004
upper GI cancer
CUI: C0814138
Disease: upper GI cancer
1 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2004 2004
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2005 2005
Cervical Adenosquamous Carcinoma
CUI: C0346202
Disease: Cervical Adenosquamous Carcinoma
1 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2005 2005
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1 2005 2005
Gastroesophageal reflux disease
CUI: C0017168
Disease: Gastroesophageal reflux disease
52 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2005 2005
premalignant lesion
CUI: C0850639
Disease: premalignant lesion
5 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1 2005 2005
Uterine Fibroids
CUI: C0042133
Disease: Uterine Fibroids
154 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2005 2005
Carcinoma breast stage IV
CUI: C0278488
Disease: Carcinoma breast stage IV
14 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2006 2006
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2006 2006
Gastric Cardia Adenocarcinoma
CUI: C1333762
Disease: Gastric Cardia Adenocarcinoma
11 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2006 2006
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2006 2006
Renal Cell Carcinoma
CUI: C0007134
Disease: Renal Cell Carcinoma
288 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2006 2006
Xeroderma Pigmentosum
CUI: C0043346
Disease: Xeroderma Pigmentosum
35 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2006 2006
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2005 2007
Breast Cancer, Familial
CUI: C0346153
Disease: Breast Cancer, Familial
91 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Cervical Intraepithelial Neoplasia
CUI: C0206708
Disease: Cervical Intraepithelial Neoplasia
29 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Hyperkeratosis
CUI: C0870082
Disease: Hyperkeratosis
19 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Keratosis
CUI: C0022593
Disease: Keratosis
10 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Melanosis
CUI: C0025209
Disease: Melanosis
23 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Melanosis coli
CUI: C0221391
Disease: Melanosis coli
5 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Myeloid Leukemia, Chronic
CUI: C0023473
Disease: Myeloid Leukemia, Chronic
115 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007
Skin lesion
CUI: C0037284
Disease: Skin lesion
52 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2007 2007