Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
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
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
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
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37