rs941759532, ERCC4

N. diseases: 11
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 0.763 0.240 16 13932175 missense variant C/G snv 0.020 1.000 2 2002 2010
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.763 0.240 16 13932175 missense variant C/G snv 0.020 1.000 2 2002 2010
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2008 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2006 2006
Malignant neoplasm of colon and/or rectum
502 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2006 2006
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2008 2008
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2002 2002
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2006 2006
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2002 2002
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2008 2008
Xeroderma Pigmentosum, Complementation Group D
111 0.763 0.240 16 13932175 missense variant C/G snv 0.010 1.000 1 2006 2006