Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs181206 0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16