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rs11078597

From SNPedia

Orientationplus
Stabilizedplus
Make rs11078597(C;C)
Make rs11078597(C;T)
Make rs11078597(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position1715069
GeneMIR22, MIR22HG, WDR81
is asnp
is mentioned by
dbSNPrs11078597
ebirs11078597
HLIrs11078597
Exacrs11078597
Varsomers11078597
Maprs11078597
PheGenIrs11078597
hapmaprs11078597
1000 genomesrs11078597
hgdprs11078597
ensemblrs11078597
gopubmedrs11078597
geneviewrs11078597
scholarrs11078597
googlers11078597
pharmgkbrs11078597
gwascentralrs11078597
openSNPrs11078597
23andMers11078597
23andMe allrs11078597
SNP Nexus

SNPshotrs11078597
SNPdbers11078597
MSV3drs11078597
GWAS Ctlgrs11078597
GMAF0.1726
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23022100OA-icon.png]
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