Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4644 0.732 0.320 14 55138217 missense variant C/A;G snv 0.35 14
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 28
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs9296068 0.925 0.200 6 33020918 intergenic variant T/G snv 0.42 2
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47