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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.878 49 2001 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2016 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.878 49 2001 2019
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 1.000 2 2014 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.500 4 2012 2018
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2008 2016
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.813 16 2003 2018
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2011 2011
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
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.921 38 2003 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2008 2018
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.900 10 2004 2018
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.921 38 2003 2019
Obesity
CUI: C0028754
Disease: Obesity
1111 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2013 2013
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2015 2015
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.900 10 2004 2018
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2012 2012
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.921 38 2003 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.842 19 2009 2020
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.020 0.500 2 2011 2019