Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs242941 0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1800044 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs12936511 0.925 0.080 17 45807036 synonymous variant C/T snv 3.1E-02 3.0E-02 5
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82