Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397509039
rs397509039
1.000 0.200 17 43092379 missense variant G/A;C snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2009 2009
dbSNP: rs397509039
rs397509039
1.000 0.200 17 43092379 missense variant G/A;C snv
Hereditary Breast and Ovarian Cancer Syndrome
0.010 1.000 1 2009 2009