Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs3748816 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs13119723 0.807 0.280 4 122297158 intron variant A/G snv 0.10 5