rs1790349
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1790349(A;A) |
Make rs1790349(A;G) |
Make rs1790349(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 71431304 |
is a | snp |
is | mentioned by |
dbSNP | rs1790349 |
dbSNP (classic) | rs1790349 |
ClinGen | rs1790349 |
ebi | rs1790349 |
HLI | rs1790349 |
Exac | rs1790349 |
Gnomad | rs1790349 |
Varsome | rs1790349 |
LitVar | rs1790349 |
Map | rs1790349 |
PheGenI | rs1790349 |
Biobank | rs1790349 |
1000 genomes | rs1790349 |
hgdp | rs1790349 |
ensembl | rs1790349 |
geneview | rs1790349 |
scholar | rs1790349 |
rs1790349 | |
pharmgkb | rs1790349 |
gwascentral | rs1790349 |
openSNP | rs1790349 |
23andMe | rs1790349 |
SNPshot | rs1790349 |
SNPdbe | rs1790349 |
MSV3d | rs1790349 |
GWAS Ctlg | rs1790349 |
GMAF | 0.2241 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23505139] An analysis of the association between the vitamin D pathway and serum 25-hydroxyvitamin D levels in a healthy Chinese population
[PMID 20418485] Genome-wide association study of circulating vitamin D levels.
[PMID 21972121] Associations between common variants in GC and DHCR7/NADSYN1 and vitamin D concentration in Chinese Hans.