Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1015443 0.925 0.160 12 10908523 missense variant T/A;C snv 4.0E-06; 0.59 2
rs3782025 0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6990313 1.000 0.080 8 11712527 intron variant G/T snv 0.14 1
rs10112596 0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
rs11250159 1.000 0.080 8 11729725 intron variant G/A;T snv 1
rs17153694 0.851 0.160 8 11730972 intron variant C/T snv 0.12 4
rs463379 0.882 0.080 5 1431049 intron variant G/C snv 0.31 3
rs6350 0.882 0.080 5 1443084 missense variant G/A;C snv 5.6E-02; 6.8E-05 3
rs17777298 1.000 0.080 5 148541962 intron variant T/A snv 0.24 1
rs10044881 1.000 0.080 5 148645656 non coding transcript exon variant T/C snv 0.17 1
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4532 0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs1799913 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs56013859 0.925 0.080 2 238276865 intron variant T/C snv 0.11 2
rs7958822 0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs4964057 0.882 0.080 12 27363909 intron variant T/G snv 0.29 3
rs2306073 0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs916264 1.000 0.080 22 36237790 intron variant A/C;T snv 1