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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs61750420 0.689 0.480 7 92501562 missense variant C/T snv 3.2E-04 3.5E-04 52
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs2228603 0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs2854116 0.807 0.200 11 116829453 upstream gene variant C/T snv 0.51 7
rs1057972 0.790 0.200 4 141733279 3 prime UTR variant A/T snv 0.54 7