Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2853669 0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs55705857 0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs5742612 0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs6470517 0.925 0.080 8 127448159 intron variant A/G snv 0.15 3
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs7837328 0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs267605077 0.925 0.080 17 7675212 missense variant A/G;T snv 3
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1056827 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs16260 0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 19
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11