rs11078597
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11078597(C;C) |
Make rs11078597(C;T) |
Make rs11078597(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 1715069 |
Gene | MIR22, MIR22HG, WDR81 |
is a | snp |
is | mentioned by |
dbSNP | rs11078597 |
dbSNP (classic) | rs11078597 |
ClinGen | rs11078597 |
ebi | rs11078597 |
HLI | rs11078597 |
Exac | rs11078597 |
Gnomad | rs11078597 |
Varsome | rs11078597 |
LitVar | rs11078597 |
Map | rs11078597 |
PheGenI | rs11078597 |
Biobank | rs11078597 |
1000 genomes | rs11078597 |
hgdp | rs11078597 |
ensembl | rs11078597 |
geneview | rs11078597 |
scholar | rs11078597 |
rs11078597 | |
pharmgkb | rs11078597 |
gwascentral | rs11078597 |
openSNP | rs11078597 |
23andMe | rs11078597 |
SNPshot | rs11078597 |
SNPdbe | rs11078597 |
MSV3d | rs11078597 |
GWAS Ctlg | rs11078597 |
GMAF | 0.1726 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23022100] |
Trait | Serum albumin level |
Title | Discovery and fine mapping of serum protein loci through transethnic meta-analysis. |
Risk Allele | C |
P-val | 1E-14 |
Odds Ratio | .02 [0.015-0.026] unit increase |