Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2412646 0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs10112596 0.925 0.120 8 11722293 intron variant A/G snv 0.83 3
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
rs2306073 0.882 0.080 12 27402904 intron variant C/T snv 0.37 4
rs17153694 0.851 0.160 8 11730972 intron variant C/T snv 0.12 4
rs6923761 0.851 0.200 6 39066296 missense variant G/A;C snv 0.23; 4.0E-06 4
rs3782025 0.882 0.080 11 113936885 intron variant G/A snv 0.55 4
rs356200 0.882 0.160 4 89747463 intron variant T/C snv 0.44 4
rs279871 0.882 0.080 4 46303716 intron variant T/C snv 0.38 5
rs1799913 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs7958822 0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
rs2066702 0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs4532 0.827 0.160 5 175443147 5 prime UTR variant C/T snv 0.68 0.72 7
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs6971 0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95