Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs10817938 0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs10491121 0.882 0.120 17 36102943 upstream gene variant G/A snv 0.32 5
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22