Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
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
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27