Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11465817 0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs1010023 0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs1419881 0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 4
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs12614 0.851 0.160 6 31946402 missense variant C/G;T snv 4.1E-06; 0.12 5
rs1054690270 0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs705382 0.827 0.200 7 95325909 upstream gene variant C/G snv 0.53 5
rs1800750
TNF
0.827 0.280 6 31575186 upstream gene variant G/A snv 1.6E-02 5
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3130542 0.827 0.160 6 31264334 downstream gene variant A/G snv 0.81 8
rs13419896 0.776 0.240 2 46329206 intron variant G/A snv 0.10 8
rs422951 0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 8
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs7453920 0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs1053005 0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs2293152 0.763 0.480 17 42329511 intron variant G/A;C;T snv 2.8E-05; 0.59; 1.6E-05 10
rs2280714 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs3024490 0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs1053004 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs61330082 0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13