Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs9943582 0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs7081476 0.851 0.120 10 26969741 intergenic variant G/C;T snv 7
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
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
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7