rs376040996, XPA

N. diseases: 7
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.
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.020 1.000 2 2004 2007
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.020 1.000 2 2004 2007
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.020 1.000 2 2004 2007
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.010 1.000 1 2017 2017
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.010 1.000 1 2017 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.010 1.000 1 2010 2010
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 0.010 1.000 1 2010 2010