Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
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
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs6971 0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs356219 0.776 0.240 4 89716450 intron variant G/A snv 0.54 9
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
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
rs7958822 0.807 0.200 12 27348173 intron variant G/A snv 0.43 6
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
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