Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 11
rs4533622 0.807 0.240 3 41200847 intron variant C/A;T snv 6