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
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 31
rs28934907 0.732 0.320 X 154032268 missense variant G/A;C snv 30
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs113994097 0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs3740066 0.724 0.440 10 99844450 missense variant C/G;T snv 2.4E-05; 0.34 20
rs61750240 0.752 0.240 X 154031020 stop gained G/A;C snv 5.5E-06 19
rs28935468 0.732 0.240 X 154030912 missense variant G/A snv 17
rs2606345 0.732 0.360 15 74724835 intron variant C/A snv 0.46 16
rs1064797102 0.827 0.120 8 91071136 splice acceptor variant A/G snv 15
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14