Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs2306073 0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs356200 0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs10112596 0.925 0.120 8 11722293 intron variant A/G snv 0.83 3