Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
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
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
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
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
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
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs153109 0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26