Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22