Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs1800759 0.925 0.120 4 99144358 intron variant T/G snv 0.49 4
rs1047383 20 8884359 3 prime UTR variant C/T snv 0.56 1
rs1650420 1.000 0.080 16 10174473 intron variant T/C snv 0.58 2
rs13438494 1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1126671 0.851 0.120 4 99127263 missense variant T/C snv 0.76 0.75 5