rs2298850
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2298850(C;C) |
Make rs2298850(C;G) |
Make rs2298850(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 4 |
Position | 71748550 |
Gene | GC |
is a | snp |
is | mentioned by |
dbSNP | rs2298850 |
dbSNP (classic) | rs2298850 |
ClinGen | rs2298850 |
ebi | rs2298850 |
HLI | rs2298850 |
Exac | rs2298850 |
Gnomad | rs2298850 |
Varsome | rs2298850 |
LitVar | rs2298850 |
Map | rs2298850 |
PheGenI | rs2298850 |
Biobank | rs2298850 |
1000 genomes | rs2298850 |
hgdp | rs2298850 |
ensembl | rs2298850 |
geneview | rs2298850 |
scholar | rs2298850 |
rs2298850 | |
pharmgkb | rs2298850 |
gwascentral | rs2298850 |
openSNP | rs2298850 |
23andMe | rs2298850 |
SNPshot | rs2298850 |
SNPdbe | rs2298850 |
MSV3d | rs2298850 |
GWAS Ctlg | rs2298850 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 27282160] GC and VDR SNPs and Vitamin D Levels in Parkinson's Disease: The Relevance to Clinical Features.
[PMID 28253304] Bone mineral density is associated with vitamin D related rs6013897 and estrogen receptor polymorphism rs4870044: The Tromsø study.
[PMID 30150596] Association between Vitamin D Deficiency and Single Nucleotide Polymorphisms in the Vitamin D Receptor and GC Genes and Analysis of Their Distribution in Mexican Postmenopausal Women.
[PMID 32537819] Association between variants in vitamin D-binding protein gene and vitamin D deficiency among pregnant women in china.