Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs28935197 0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 10
rs2074192 0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs2070951 0.776 0.320 4 148436862 splice region variant G/A;C snv 4.2E-06; 0.53 9
rs104894503 0.776 0.160 15 63060899 missense variant G/A snv 1.6E-05 2.8E-05 9
rs2106809 0.827 0.120 X 15599938 intron variant A/G snv 0.19 8
rs2296545 0.851 0.160 10 88583080 missense variant C/G;T snv 0.46 8
rs142000963 0.807 0.240 1 156138719 missense variant C/A;T snv 1.2E-03 8
rs869312687 0.925 0.080 1 155910695 missense variant T/G snv 8
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 7
rs59026483 0.827 0.160 1 156134457 missense variant C/T snv 7.0E-06 7
rs121908596 0.807 0.240 15 66436837 missense variant G/A;T snv 7
rs397516005 0.827 0.120 11 47333566 stop gained G/A snv 8.4E-06 2.8E-05 5
rs387907267 0.851 0.120 11 47335120 stop gained G/A snv 1.2E-05 2.8E-05 4
rs397516037 0.851 0.120 11 47332189 stop gained G/A snv 8.0E-06 4
rs1060501439 0.925 0.080 14 23424938 missense variant T/A snv 4
rs755492182 0.882 0.080 1 236735677 missense variant C/T snv 3
rs4966014 0.882 0.200 15 98704789 intron variant C/G;T snv 3
rs201278114 0.925 0.120 11 47352635 missense variant C/A;G snv 4.3E-06; 3.0E-04 3
rs1436109 1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02 3
rs148158093 0.925 0.200 X 101403828 missense variant G/A snv 2.2E-04 4.0E-04 3
rs1277204441
ACE
0.925 0.080 17 63479775 missense variant C/T snv 7.0E-06 2
rs1050606 1.000 0.080 4 121696891 5 prime UTR variant A/C snv 0.50 2
rs768079285 1.000 0.080 10 20840824 frameshift variant T/- delins 8.0E-06 2