Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs368087026 0.637 0.520 21 45530890 missense variant G/A snv 33