Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44