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rs11160190

From SNPedia

Orientationplus
Stabilizedplus
Make rs11160190(A;A)
Make rs11160190(A;G)
Make rs11160190(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position94546047
is asnp
is mentioned by
dbSNPrs11160190
dbSNP (classic)rs11160190
ClinGenrs11160190
ebirs11160190
HLIrs11160190
Exacrs11160190
Gnomadrs11160190
Varsomers11160190
LitVarrs11160190
Maprs11160190
PheGenIrs11160190
Biobankrs11160190
1000 genomesrs11160190
hgdprs11160190
ensemblrs11160190
geneviewrs11160190
scholarrs11160190
googlers11160190
pharmgkbrs11160190
gwascentralrs11160190
openSNPrs11160190
23andMers11160190
SNPshotrs11160190
SNPdbers11160190
MSV3drs11160190
GWAS Ctlgrs11160190
GMAF0.3329
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22907691]
Trait Vaspin levels
Title Genetic variation in the vaspin gene affects circulating serum vaspin concentrations.
Risk Allele G
P-val 4E-41
Odds Ratio .04 [NR] unit decrease