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: rs1042028
rs1042028
0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.010 1.000 1 2014 2014