Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs753152 0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140