Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs441 0.882 0.200 12 111791045 intron variant T/C snv 0.18 4
rs1650420 1.000 0.080 16 10174473 intron variant T/C snv 0.58 2
rs3735451 7 99758352 intron variant T/C snv 0.31 1
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs13438494 1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1800759 0.925 0.120 4 99144358 intron variant T/G snv 0.49 4