Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16