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
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
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
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs2227306 0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs143383 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17