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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
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
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs28934906 0.716 0.320 X 154031355 missense variant G/A snv 46
rs780533096 0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs121918455 0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs1554208945 0.752 0.240 6 87260207 missense variant A/C snv 26
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs61749721 0.732 0.200 X 154031065 stop gained G/A snv 17
rs1555247672 0.827 0.200 12 116007542 stop gained G/A snv 14