Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1562444 0.925 0.120 11 92982683 3 prime UTR variant G/A snv 0.55 2
rs2165667 0.925 0.040 4 186540475 intron variant A/G;T snv 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs224222 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 15
rs104895094 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs4958847 0.807 0.120 5 150860025 intron variant G/A snv 0.25 8
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 7
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs848 0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 8
rs3024498 0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111