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: rs754215085
rs754215085
1 1.000 0.080 4 105276407 missense variant G/A snv 5.7E-05 1.4E-05 0.700 0
dbSNP: rs761064473
rs761064473
1 1.000 0.080 2 25240717 missense variant C/G;T snv 1.2E-05 0.700 0
dbSNP: rs771761785
rs771761785
1 1.000 0.080 4 105243757 missense variant G/A;C snv 6.4E-06 0.700 0