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.
Congenital chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.060 1.000 6 2004 2012
Differentiated Thyroid Gland Carcinoma
CUI: C1337013
Disease: Differentiated Thyroid Gland Carcinoma
80 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.060 0.667 6 2009 2016
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.060 0.500 6 2005 2014
Nasopharyngeal carcinoma
CUI: C2931822
Disease: Nasopharyngeal carcinoma
320 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.060 0.667 6 2006 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
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
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.050 0.600 5 2007 2015
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2004 2013
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2004 2013
Lip and Oral Cavity Carcinoma
CUI: C0220641
Disease: Lip and Oral Cavity Carcinoma
172 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2013 2014
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
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2004 2013
Malignant neoplasm of mouth
CUI: C0153381
Disease: Malignant neoplasm of mouth
184 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2013 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 1.000 4 2006 2016
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
103 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2012 2019
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 1.000 4 2006 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
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
145 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2012 2019
Thyroid Neoplasm
CUI: C0040136
Disease: Thyroid Neoplasm
135 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.040 0.750 4 2012 2019
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
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 0.667 3 2004 2011
Carcinoma of larynx
CUI: C0595989
Disease: Carcinoma of larynx
65 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2014 2016
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2018
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2012 2016
Childhood Leukemia
CUI: C1332977
Disease: Childhood Leukemia
140 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.030 1.000 3 2013 2015