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.
Male infertility
CUI: C0021364
Disease: Male infertility
146 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 0.500 2 2017 2018
Malignant Female Reproductive System Neoplasm
CUI: C0699889
Disease: Malignant Female Reproductive System Neoplasm
5 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 0.500 2 2017 2018
Malignant neoplasm of liver
CUI: C0345904
Disease: Malignant neoplasm of liver
88 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2013 2018
ovarian neoplasm
CUI: C0919267
Disease: ovarian neoplasm
757 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2013 2018
Acute mucositis
CUI: C1290073
Disease: Acute mucositis
1 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2018 2018
Adult Liver Carcinoma
CUI: C0220630
Disease: Adult Liver Carcinoma
72 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2018 2018
Liver and Intrahepatic Biliary Tract Carcinoma
CUI: C0279000
Disease: Liver and Intrahepatic Biliary Tract Carcinoma
73 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2018 2018
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.960 25 2004 2017
Glioma
CUI: C0017638
Disease: Glioma
353 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.933 15 2010 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.800 15 2003 2017
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.050 0.600 5 2007 2017
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.050 1.000 5 2012 2017
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
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
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Genital Neoplasms, Female
CUI: C0017416
Disease: Genital Neoplasms, Female
4 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Nasal Polyps
CUI: C0027430
Disease: Nasal Polyps
34 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Squamous cell carcinoma of skin
CUI: C0553723
Disease: Squamous cell carcinoma of skin
92 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Urologic Neoplasms
CUI: C0042076
Disease: Urologic Neoplasms
4 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2017 2017
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.960 25 2004 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.833 24 2004 2016
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.615 13 2004 2016
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.615 13 2004 2016