rs10877012
| Orientation | plus |
| Stabilized | plus |
| Make rs10877012(G;G) |
| Make rs10877012(G;T) |
| Make rs10877012(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 57768302 |
| Gene | CYP27B1, METTL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10877012 |
| dbSNP (classic) | rs10877012 |
| ClinGen | rs10877012 |
| ebi | rs10877012 |
| HLI | rs10877012 |
| Exac | rs10877012 |
| Gnomad | rs10877012 |
| Varsome | rs10877012 |
| LitVar | rs10877012 |
| Map | rs10877012 |
| PheGenI | rs10877012 |
| Biobank | rs10877012 |
| 1000 genomes | rs10877012 |
| hgdp | rs10877012 |
| ensembl | rs10877012 |
| geneview | rs10877012 |
| scholar | rs10877012 |
| rs10877012 | |
| pharmgkb | rs10877012 |
| gwascentral | rs10877012 |
| openSNP | rs10877012 |
| 23andMe | rs10877012 |
| SNPshot | rs10877012 |
| SNPdbe | rs10877012 |
| MSV3d | rs10877012 |
| GWAS Ctlg | rs10877012 |
| GMAF | 0.3545 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
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[PMID 19951419
] Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis
[PMID 20363324] A systematic review of the association between common single nucleotide polymorphisms and 25-hydroxyvitamin D concentrations
[PMID 20394945] Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment
[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 19956108] Analysis of 55 autoimmune disease and type II diabetes loci: further confirmation of chromosomes 4q27, 12q13.2 and 12q24.13 as type I diabetes loci, and support for a new locus, 12q13.3-q14.1.
[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 21145801] Vitamin D deficiency and a CYP27B1-1260 promoter polymorphism are associated with chronic hepatitis C and poor response to interferon-alfa based therapy.
[PMID 21358824] Prostate cancer susceptibility Loci identified on chromosome 12 in African Americans.
[PMID 22559001] Impaired Vitamin D activation and association with CYP24A1 haplotypes in differentiated thyroid carcinoma.
[PMID 22690899] Impaired Vitamin D Activation and Association with CYP24A1 Haplotypes in Differentiated Thyroid Carcinoma.
[PMID 23416105] Vitamin D status and gene transcription in immune cells
[PMID 24073221] Influence of Vitamin D-Related Gene Polymorphisms (CYP27B and VDR) on the Response to Interferon/Ribavirin Therapy in Chronic Hepatitis C
[PMID 23923033] The association between plasma 25-hydroxyvitamin D and subgroups in age-related macular degeneration: a cross-sectional study
[PMID 25628655] The Associations of Novel Vitamin D3 Metabolic Gene CYP27A1 Polymorphism, Adiponectin/Leptin Ratio, and Metabolic Syndrome in Middle-Aged Taiwanese Males
[PMID 31959263] Vitamin D related genes and cardiometabolic markers in healthy children: a Mendelian randomization study.
[PMID 32127688] CYP27B1 as an instrument gene to investigate the causal relationship between vitamin D deficiency and obesity: a family-based study.
[PMID 32260235] CYP27B1 Gene Polymorphism rs10877012 in Patients Diagnosed with Colorectal Cancer.
