Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
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
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs2269426 0.807 0.280 6 32108722 intron variant G/A snv 0.35 10
rs406936 0.882 0.240 6 31965384 intron variant G/A snv 0.19 3
rs4151659 0.925 0.160 6 31950687 missense variant A/G snv 1.1E-02 1.8E-02 3
rs8056814 0.925 0.160 16 75218429 upstream gene variant G/A snv 0.16 2