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.
Carcinoma, Transitional Cell
CUI: C0007138
Disease: Carcinoma, Transitional Cell
12 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2014 2015
Cancer of Nasopharynx
CUI: C0238301
Disease: Cancer of Nasopharynx
12 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1 2014 2014
Malignant mesothelioma
CUI: C0345967
Disease: Malignant mesothelioma
12 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2012 2012
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
Adult Hepatocellular Carcinoma
CUI: C0279607
Disease: Adult Hepatocellular Carcinoma
14 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
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
Age-related cataract
CUI: C0036646
Disease: Age-related cataract
15 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2015 2015
Dermatitis
CUI: C0011603
Disease: Dermatitis
16 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
Lymphopenia
CUI: C0024312
Disease: Lymphopenia
16 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2015 2015
Oral Mucositis
CUI: C1568868
Disease: Oral Mucositis
16 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
Childhood Hepatocellular Carcinoma
CUI: C0279606
Disease: Childhood Hepatocellular Carcinoma
17 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
polyps
CUI: C0032584
Disease: polyps
18 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2011 2011
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
Ovarian Carcinoma
CUI: C0029925
Disease: Ovarian Carcinoma
19 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2015 2015
Stomatitis
CUI: C0038362
Disease: Stomatitis
22 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
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
Skin carcinoma
CUI: C0699893
Disease: Skin carcinoma
24 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2002 2017
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
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
Laryngeal Squamous Cell Carcinoma
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
30 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2003 2013
Xeroderma pigmentosum, group G
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
31 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2009 2009
Familial multiple trichoepitheliomata
CUI: C1275122
Disease: Familial multiple trichoepitheliomata
32 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2008 2008
Fuchs Endothelial Dystrophy
CUI: C0016781
Disease: Fuchs Endothelial Dystrophy
32 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2015 2015
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2011 2011
Niemann-Pick Disease, Type C
CUI: C0220756
Disease: Niemann-Pick Disease, Type C
33 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2014 2014