Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs886041065 0.677 0.600 2 25743913 frameshift variant G/- delins 43
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs34757931 0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 26
rs1555745467 0.752 0.240 19 13262771 missense variant C/A snv 23
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18
rs6746030 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs211037 0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31 14
rs201439531 0.827 0.200 10 49664880 missense variant C/G snv 7.0E-06 11
rs769234940 0.827 0.200 10 49627735 missense variant C/T snv 1.6E-05 2.8E-05 11
rs61738009 0.827 0.080 8 67483807 stop gained C/A;T snv 4.0E-06; 2.0E-03 2.5E-03 11
rs1559193213 0.807 0.160 2 166036149 frameshift variant -/G delins 11
rs121909673 0.776 0.080 5 162093965 missense variant G/A snv 10
rs755604487 0.790 0.200 6 79026079 stop gained G/A;C snv 10