Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2255336 0.827 0.200 12 10379727 missense variant T/C snv 0.81 0.74 5
rs2617160 1.000 0.080 12 10392998 intron variant A/C;T snv 1
rs11053781 1.000 0.080 12 10384670 intron variant C/G;T snv 1