Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs7195830 0.851 0.080 16 88643304 3 prime UTR variant A/G snv 0.62 0.69 6
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7