Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs760761 0.882 0.080 6 15650901 intron variant G/A snv 0.26 4
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
rs528732638 0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 5
rs61888800 0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs766020740 0.851 0.120 22 19963644 missense variant C/A snv 4.0E-06 5
rs794727961 0.851 0.080 12 2512979 missense variant G/A snv 5
rs9825823 0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
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
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
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8