Have questions? Visit https://www.reddit.com/r/SNPedia

rs739837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs739837(G;T)
Make rs739837(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position47844438
GeneVDR
is asnp
is mentioned by
dbSNPrs739837
dbSNP (old)rs739837
ClinGenrs739837
ebirs739837
HLIrs739837
Exacrs739837
Gnomadrs739837
Varsomers739837
Maprs739837
PheGenIrs739837
Biobankrs739837
1000 genomesrs739837
hgdprs739837
ensemblrs739837
gopubmedrs739837
geneviewrs739837
scholarrs739837
googlers739837
pharmgkbrs739837
gwascentralrs739837
openSNPrs739837
23andMers739837
23andMe allrs739837
SNP Nexus

SNPshotrs739837
SNPdbers739837
MSV3drs739837
GWAS Ctlgrs739837
GMAF0.4803
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 19105801OA-icon.png] rs739837 fair skin (OR=1.31, p=0.048)

[PMID 19454612OA-icon.png] Vitamin D pathway gene variants and prostate cancer risk.

[PMID 20015871OA-icon.png] Pharmacogenetic risk factors for altered bone mineral density and body composition in pediatric acute lymphoblastic leukemia.


[PMID 26448018OA-icon.png] Variants in Vitamin D Binding Protein Gene Are Associated With Gestational Diabetes Mellitus


[PMID 26453801] Vitamin D Receptor Genetic Polymorphism Is Significantly Associated with Risk of Type 2 Diabetes Mellitus in Chinese Han Population


ClinVar
Risk rs739837(T;T)
Alt rs739837(T;T)
Reference Rs739837(G;G)
Significance Probable-non-pathogenic
Disease Vitamin D-Dependent Rickets
Variation info
Gene VDR
CLNDBN Vitamin D-Dependent Rickets
Reversed 0
HGVS NC_000012.11:g.48238221G>T
CLNSRC
CLNACC RCV000351615.1,