rs2189480
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2189480(A;A) |
Make rs2189480(A;C) |
Make rs2189480(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 47870045 |
Gene | VDR |
is a | snp |
is | mentioned by |
dbSNP | rs2189480 |
dbSNP (classic) | rs2189480 |
ClinGen | rs2189480 |
ebi | rs2189480 |
HLI | rs2189480 |
Exac | rs2189480 |
Gnomad | rs2189480 |
Varsome | rs2189480 |
LitVar | rs2189480 |
Map | rs2189480 |
PheGenI | rs2189480 |
Biobank | rs2189480 |
1000 genomes | rs2189480 |
hgdp | rs2189480 |
ensembl | rs2189480 |
geneview | rs2189480 |
scholar | rs2189480 |
rs2189480 | |
pharmgkb | rs2189480 |
gwascentral | rs2189480 |
openSNP | rs2189480 |
23andMe | rs2189480 |
SNPshot | rs2189480 |
SNPdbe | rs2189480 |
MSV3d | rs2189480 |
GWAS Ctlg | rs2189480 |
GMAF | 0.4403 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 23413917] Serum 25-hydroxyvitamin D3 levels and vitamin D receptor variants in melanoma patients from the Mediterranean area of Barcelona: 25-hydroxyvitamin D3 levels and VDR variants in melanoma patients from Barcelona
[PMID 17903296] Genome-wide association with bone mass and geometry in the Framingham Heart Study.
[PMID 19956101] Overview of the Rapid Response data.
[PMID 19956103] Association analyses of the vitamin D receptor gene in 1654 families with type I diabetes.
[PMID 30683435] Serum vitamin D deficiency and vitamin D receptor gene polymorphism are associated with increased risk of cardiovascular disease in a Chinese rural population.
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2d