Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7854303 1.000 0.200 9 5557672 missense variant T/C snv 1.00 1.00 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 24
rs1048709 0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1554286 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs27044 0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 5
rs2227981 0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs2617170 1.000 0.200 12 10408358 missense variant T/C snv 0.63 0.61 1
rs30187 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 14
rs2293152 0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111