Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1110839 0.807 0.120 2 113236840 non coding transcript exon variant G/A;C;T snv 6
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11543848 0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1266828 0.807 0.120 6 52243264 intron variant G/A snv 0.75 6
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119