Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47