Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 11
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs10877012 0.763 0.280 12 57768302 intron variant G/C;T snv 10
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs389884 0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 10
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs9257809 0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 10
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 10
rs694739 0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 9
rs3177928 0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 8
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 7
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7