Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227981 0.763 0.400 2 241851121 synonymous variant A/C;G snv 1.6E-04; 0.63 12
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs10515746 0.925 0.240 5 157109557 intron variant A/C;T snv 2
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3853839 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 10
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1234315 0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs1800450 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs2280714 0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10