Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs17622378 0.790 0.200 5 132442760 intron variant A/G snv 0.28 8