Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs60652225
rs60652225
4 0.851 0.200 1 156130679 missense variant T/C;G snv 0.700 0
dbSNP: rs60864230
rs60864230
7 0.790 0.280 1 156130658 missense variant G/A;C;T snv 4.0E-06 0.700 0
dbSNP: rs730882262
rs730882262
4 0.851 0.160 1 156135293 missense variant T/C;G snv 0.700 0