Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4717806 0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
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
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs751141 0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs753152 0.882 0.160 17 42761487 intron variant T/G snv 0.12 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93