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.
Endometriosis
CUI: C0014175
Disease: Endometriosis
274 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2007 2017
Glaucoma, Primary Open Angle
CUI: C0339573
Disease: Glaucoma, Primary Open Angle
222 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2011 2015
leukemia
CUI: C0023418
Disease: leukemia
144 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2015
Malignant neoplasm of larynx
CUI: C0007107
Disease: Malignant neoplasm of larynx
50 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2014 2016
Malignant neoplasm of ovary
CUI: C1140680
Disease: Malignant neoplasm of ovary
315 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2018
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 0.667 3 2004 2011
melanoma
CUI: C0025202
Disease: melanoma
515 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 0.667 3 2006 2016
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2010 2011
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
Sporadic Breast Carcinoma
CUI: C1336076
Disease: Sporadic Breast Carcinoma
46 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2007 2015
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 0.333 3 2002 2009
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
82 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2005 2015
Adenocarcinoma
CUI: C0001418
Disease: Adenocarcinoma
168 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2005 2010
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
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2013 2016
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
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 0.500 2 2007 2012
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2005 2008
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
Cataract
CUI: C0086543
Disease: Cataract
124 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2011 2015
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2013 2016
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2012 2015
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
291 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2009 2012
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2009 2013
Cutaneous Melanoma
CUI: C0151779
Disease: Cutaneous Melanoma
248 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2006 2016