Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
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
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1234315 0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56