Gene: VDR ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1544410
rs1544410
VDR
78 0.542 0.760 12 47846052 intron variant C/A;G;T snv 0.040 1.000 4 2014 2018
dbSNP: rs7975232
rs7975232
VDR
56 0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 0.030 1.000 3 2015 2019
dbSNP: rs2228570
rs2228570
VDR
99 0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 0.020 1.000 2 2013 2019
dbSNP: rs121909798
rs121909798
VDR
2 0.925 0.200 12 47846444 missense variant G/C snv 0.010 1.000 1 2015 2015
dbSNP: rs145438594
rs145438594
VDR
1 1.000 0.080 12 47879073 missense variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs2239185
rs2239185
VDR
6 0.807 0.320 12 47850776 intron variant G/A snv 0.54 0.010 1.000 1 2014 2014
dbSNP: rs3782905
rs3782905
VDR
3 0.882 0.200 12 47872384 intron variant G/C snv 0.29 0.010 1.000 1 2014 2014
dbSNP: rs731236
rs731236
VDR
81 0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 0.010 1.000 1 2019 2019
dbSNP: rs764054471
rs764054471
VDR
2 0.925 0.160 12 47879101 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 2013 2013