Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs2242446 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs242941 0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs738499 0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs9722 0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs120074175 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs1415125856 0.827 0.120 11 27658550 splice region variant G/A snv 4.0E-06 2.1E-05 7
rs1818879 0.827 0.120 7 22733108 downstream gene variant G/A;C snv 7
rs2522833 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1545843 0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs2619522 0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs1106634 0.851 0.080 8 20208538 intron variant G/A;C;T snv 0.18 5
rs11904814 0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs12912233 0.851 0.120 15 60974897 intron variant C/T snv 0.38 5
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs4648308 0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27 5