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.
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
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
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.750 16 2002 2018
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.750 16 2002 2018
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
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
Adenocarcinoma of pancreas
CUI: C0281361
Disease: Adenocarcinoma of pancreas
138 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.010 1.000 1 2002 2002
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
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
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
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
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
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
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
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
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.867 15 2004 2015
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
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.583 12 2004 2016
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
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
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
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