Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
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
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs1043210477 0.701 0.520 3 49358250 missense variant G/A snv 19
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16