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rs4949316

From SNPedia

Orientationplus
Stabilizedplus
Make rs4949316(C;C)
Make rs4949316(C;G)
Make rs4949316(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position30842746
is asnp
is mentioned by
dbSNPrs4949316
dbSNP (classic)rs4949316
ClinGenrs4949316
ebirs4949316
HLIrs4949316
Exacrs4949316
Gnomadrs4949316
Varsomers4949316
LitVarrs4949316
Maprs4949316
PheGenIrs4949316
Biobankrs4949316
1000 genomesrs4949316
hgdprs4949316
ensemblrs4949316
geneviewrs4949316
scholarrs4949316
googlers4949316
pharmgkbrs4949316
gwascentralrs4949316
openSNPrs4949316
23andMers4949316
SNPshotrs4949316
SNPdbers4949316
MSV3drs4949316
GWAS Ctlgrs4949316
GMAF0.3815
Max Magnitude0
? (C;C) (C;G) (G;G) 28


GWAS snp
PMID [PMID 23319000]
Trait Metabolite levels (5-HIAA)
Title Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Risk Allele G
P-val 9E-6
Odds Ratio .21 unit increase