Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs2854746 0.752 0.200 7 45921046 missense variant G/A;C;T snv 0.38 13
rs3110697 0.827 0.160 7 45915430 intron variant A/G snv 0.58 6