rs739837

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs739837(G;T)

Make rs739837(T;T)

Reference

GRCh38 38.1/141

Chromosome

12

Position

47844438

Gene

VDR

is a	snp
is	mentioned by
dbSNP	rs739837
dbSNP (classic)	rs739837
ClinGen	rs739837
ebi	rs739837
HLI	rs739837
Exac	rs739837
Gnomad	rs739837
Varsome	rs739837
LitVar	rs739837
Map	rs739837
PheGenI	rs739837
Biobank	rs739837
1000 genomes	rs739837
hgdp	rs739837
ensembl	rs739837
geneview	rs739837
scholar	rs739837
google	rs739837
pharmgkb	rs739837
gwascentral	rs739837
openSNP	rs739837
23andMe	rs739837
SNPshot	rs739837
SNPdbe	rs739837
MSV3d	rs739837
GWAS Ctlg	rs739837

GMAF

0.4803

Max Magnitude

0

?

(G;G) (G;T) (T;T)

28

[PMID 19105801 ] rs739837 fair skin (OR=1.31, p=0.048)

[PMID 19454612 ] Vitamin D pathway gene variants and prostate cancer risk.

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

[PMID 26448018 ] 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,

[PMID 30119682 ] Vitamin D receptor polymorphism rs2228570 is significantly associated with risk of dyslipidemia and serum LDL levels in Chinese Han population.

[PMID 33219423] Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome.