Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1235162 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs2523987 0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs2844773 0.882 0.240 6 30239718 intron variant C/A snv 0.11 3
rs3094127 0.925 0.200 6 30729670 intron variant A/G snv 0.27 3
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs3129791 0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 5
rs3130380 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs3130564 0.790 0.360 6 31133897 intron variant C/T snv 0.14 7
rs3131379 0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 10
rs3132610 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs3132685 0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs3817963 0.776 0.360 6 32400310 intron variant T/C snv 0.25 8
rs558702 0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
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
rs1794282 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 6
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs3130544 0.807 0.360 6 31090563 intergenic variant C/A snv 7.4E-02 10
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6