Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs743572 0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs333 0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs3803185 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 19
rs2853677 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs9282858 0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16