Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116