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: rs121913386
rs121913386
7 0.807 0.120 9 21971018 missense variant G/A;T snv 0.700 0
dbSNP: rs754806883
rs754806883
3 0.925 0.160 9 21971063 missense variant C/A;G;T snv 4.3E-06; 8.5E-06 0.700 0
dbSNP: rs757497674
rs757497674
1 1.000 0.080 9 21970958 missense variant G/A snv 4.1E-06 0.700 0