Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs20417 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2292832 0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs5742909 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
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
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105