Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs776746 0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs1800630 0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs1861494 0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs11674595 0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs2243115 0.776 0.320 3 159988493 intron variant T/G snv 0.10 12
rs2060793 0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs2107538 0.763 0.360 17 35880776 5 prime UTR variant C/T snv 0.27 11
rs7453920 0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs414171 0.790 0.200 3 50612068 5 prime UTR variant A/G;T snv 9
rs1061624 0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs3024498 0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs4851527 0.790 0.160 2 102005914 intron variant A/G snv 0.63 7