Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
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
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
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs3212948 0.776 0.160 19 45421104 intron variant G/C snv 0.53 10
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs2241715 0.851 0.120 19 41350981 5 prime UTR variant A/C snv 0.68 4