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rs184891496

From SNPedia

Orientationplus
Stabilizedplus
Make rs184891496(C;C)
Make rs184891496(C;T)
Make rs184891496(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position38750582
is asnp
is mentioned by
dbSNPrs184891496
ClinGenrs184891496
ebirs184891496
HLIrs184891496
Exacrs184891496
Varsomers184891496
Maprs184891496
PheGenIrs184891496
hapmaprs184891496
1000 genomesrs184891496
hgdprs184891496
ensemblrs184891496
gopubmedrs184891496
geneviewrs184891496
scholarrs184891496
googlers184891496
pharmgkbrs184891496
gwascentralrs184891496
openSNPrs184891496
23andMers184891496
23andMe allrs184891496
SNP Nexus

SNPshotrs184891496
SNPdbers184891496
MSV3drs184891496
GWAS Ctlgrs184891496
GMAF0.07622
Max Magnitude
GWAS snp
PMID [PMID 23319000]
Trait Metabolite levels (HVA/MHPG ratio)
Title Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
Risk Allele C
P-val 7E-6
Odds Ratio .28 unit increase