Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3092920 0.925 0.160 X 136661832 downstream gene variant G/T snv 0.23 2
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs4553808 0.672 0.320 2 203866282 upstream gene variant A/G;T snv 0.16 28
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs4415345 1.000 0.040 8 7057895 upstream gene variant G/A;C snv 1
rs4610776 1.000 0.040 8 7057155 upstream gene variant A/T snv 0.26 1
rs1367967034 1.000 0.040 16 50707959 splice region variant A/G snv 4.0E-06 2
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs9277534 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 7
rs37972 0.851 0.160 7 7967878 3 prime UTR variant T/A;C snv 5
rs17114808 0.925 0.040 10 102631528 3 prime UTR variant C/A;G;T snv 2
rs3004070 1.000 0.040 6 39902176 3 prime UTR variant T/A snv 0.51 1
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs1238539471 1.000 0.040 16 50710637 synonymous variant A/G snv 7.0E-06 2
rs2302217 1.000 0.040 19 498524 synonymous variant A/C;G snv 1.6E-05; 0.51 1
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs2278293 0.882 0.040 7 128400698 non coding transcript exon variant C/T snv 0.47 3
rs2278294 0.882 0.080 7 128400645 non coding transcript exon variant C/T snv 0.38 3
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25