Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs116446171 0.851 0.160 6 484453 downstream gene variant C/G snv 2.3E-02 4
rs6773854 1.000 0.120 3 187931631 downstream gene variant T/C snv 0.23 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs140522 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs3758391 0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs3957357 0.807 0.280 6 52803889 upstream gene variant A/G snv 0.63 7
rs2844484 0.807 0.320 6 31568447 upstream gene variant A/G snv 0.64 6
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs764562217 0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs3025684 1.000 0.120 16 3745362 splice region variant G/A snv 7.7E-02 0.15 2
rs4733601 1.000 0.120 8 128257220 TF binding site variant A/G snv 0.41 1
rs2066847 0.716 0.400 16 50729868 frameshift variant C/-;CC delins 1.5E-02 18
rs758653954
EFS
0.925 0.120 14 23357350 frameshift variant -/C delins 4.0E-06; 8.0E-06 2
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
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
rs2279115 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs1164376164 0.851 0.200 7 87601024 5 prime UTR variant A/G snv 6
rs1800683 0.807 0.240 6 31572294 5 prime UTR variant G/A;C snv 0.39 6
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28