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
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs3766871 0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs57045855 0.882 0.040 1 156134464 missense variant A/G;T snv 6
rs61195471 0.827 0.160 1 156134496 missense variant G/A snv 6
rs12564445 0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs567798234 0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
rs121918598 0.851 0.080 1 237648523 missense variant G/A;C snv 4
rs1739843 0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs198358 0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs61661343 0.851 0.040 1 156130687 missense variant T/C snv 4
rs10927887 0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs1253810269 0.882 0.080 1 26696971 missense variant G/A snv 7.0E-06 3
rs188344082 1.000 0.040 1 18783262 intergenic variant G/A snv 1.8E-02 3
rs61823501 1.000 0.040 1 184396836 intron variant C/T snv 0.12 3
rs74056623 1.000 0.040 1 18784584 intergenic variant G/A snv 8.3E-02 3
rs74056624 1.000 0.040 1 18790006 intergenic variant G/A snv 2.3E-02 3
rs749303395 0.882 0.040 1 114680329 missense variant G/A;C snv 8.0E-06; 4.0E-06 3
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19