Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs74315452 0.732 0.160 21 31667356 missense variant T/C snv 12
rs3849942 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs363371 0.882 0.120 10 117226885 TF binding site variant G/A snv 0.19 5
rs2814707 0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 4