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
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1386494 0.790 0.120 12 71958763 intron variant T/C;G snv 0.82 7