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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
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
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs1800477 0.763 0.480 18 63318540 missense variant C/T snv 1.8E-02 4.9E-03 12
rs10814325 0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7