rs10519951
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs10519951(A;A) |
Make rs10519951(A;G) |
Make rs10519951(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 148280467 |
Gene | NR3C2 |
is a | snp |
is | mentioned by |
dbSNP | rs10519951 |
dbSNP (classic) | rs10519951 |
ClinGen | rs10519951 |
ebi | rs10519951 |
HLI | rs10519951 |
Exac | rs10519951 |
Gnomad | rs10519951 |
Varsome | rs10519951 |
LitVar | rs10519951 |
Map | rs10519951 |
PheGenI | rs10519951 |
Biobank | rs10519951 |
1000 genomes | rs10519951 |
hgdp | rs10519951 |
ensembl | rs10519951 |
geneview | rs10519951 |
scholar | rs10519951 |
rs10519951 | |
pharmgkb | rs10519951 |
gwascentral | rs10519951 |
openSNP | rs10519951 |
23andMe | rs10519951 |
SNPshot | rs10519951 |
SNPdbe | rs10519951 |
MSV3d | rs10519951 |
GWAS Ctlg | rs10519951 |
GMAF | 0.1708 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 23334005] Confounding and Heterogeneity in Genetic Association Studies with Admixed Populations