Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs9943582 0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4