Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
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
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10
rs843706 0.807 0.160 2 54253232 3 prime UTR variant C/A snv 0.42 6
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
rs2241715 0.851 0.120 19 41350981 5 prime UTR variant A/C snv 0.68 4
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs937283 0.716 0.200 12 68808384 5 prime UTR variant A/G snv 0.37 19
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs230525 0.882 0.080 4 102537720 non coding transcript exon variant G/A snv 0.69 4
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1051861187 0.827 0.080 7 87409385 missense variant A/G snv 6
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1330010954 0.882 0.080 8 13094897 missense variant C/T snv 4.0E-06 4
rs1476081557 0.882 0.080 19 35721455 missense variant G/T snv 7.0E-06 3
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174