Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 10
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 10
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 6
rs4533622 0.807 0.240 3 41200847 intron variant C/A;T snv 6