rs4646536
Orientation | minus |
Stabilized | minus |
Make rs4646536(C;C) |
Make rs4646536(C;T) |
Make rs4646536(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 57764205 |
Gene | CYP27B1 |
is a | snp |
is | mentioned by |
dbSNP | rs4646536 |
dbSNP (classic) | rs4646536 |
ClinGen | rs4646536 |
ebi | rs4646536 |
HLI | rs4646536 |
Exac | rs4646536 |
Gnomad | rs4646536 |
Varsome | rs4646536 |
LitVar | rs4646536 |
Map | rs4646536 |
PheGenI | rs4646536 |
Biobank | rs4646536 |
1000 genomes | rs4646536 |
hgdp | rs4646536 |
ensembl | rs4646536 |
geneview | rs4646536 |
scholar | rs4646536 |
rs4646536 | |
pharmgkb | rs4646536 |
gwascentral | rs4646536 |
openSNP | rs4646536 |
23andMe | rs4646536 |
SNPshot | rs4646536 |
SNPdbe | rs4646536 |
MSV3d | rs4646536 |
GWAS Ctlg | rs4646536 |
GMAF | 0.4054 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23149444] Negative Predictive Value of IL28B, SLC28A2, and CYP27B1 SNPs and Low RBV Plasma Exposure for Therapeutic Response to PEG/IFN-RBV Treatment
[PMID 22576141] No association of vitamin D metabolism-related polymorphisms and melanoma risk as well as melanoma prognosis: a case-control study
[PMID 23979957] Association between vitamin D metabolism gene polymorphisms and risk of islet autoimmunity and progression to type 1 diabetes: the diabetes autoimmunity study in the young (DAISY)
[PMID 16600026] Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway.
[PMID 17606874] Association of the vitamin D metabolism gene CYP27B1 with type 1 diabetes.
[PMID 18593774] Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans.
[PMID 18689381] Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis.
[PMID 19706847] Vitamin D related genes, CYP24A1 and CYP27B1, and colon cancer risk.
[PMID 19783860] A rare haplotype of the vitamin D receptor gene is protective against diabetic nephropathy.
[PMID 20648053] Confirmation of association between multiple sclerosis and CYP27B1.
[PMID 21107545] Contribution of a common variant in the promoter of the 1-alpha-hydroxylase gene (CYP27B1) to fracture risk in the elderly.
[PMID 22690899] Impaired vitamin D activation and association with CYP24A1 haplotypes in differentiated thyroid carcinoma.
[PMID 26303648] Association of vdr, cyp27b1, cyp24a1 and mthfr gene polymorphisms with oral lichen planus risk
[PMID 32127688] CYP27B1 as an instrument gene to investigate the causal relationship between vitamin D deficiency and obesity: a family-based study.