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rs1902272

From SNPedia

Orientationplus
Stabilizedplus
Make rs1902272(C;C)
Make rs1902272(C;T)
Make rs1902272(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position31551178
is asnp
is mentioned by
dbSNPrs1902272
ebirs1902272
HLIrs1902272
Exacrs1902272
Varsomers1902272
Maprs1902272
PheGenIrs1902272
hapmaprs1902272
1000 genomesrs1902272
hgdprs1902272
ensemblrs1902272
gopubmedrs1902272
geneviewrs1902272
scholarrs1902272
googlers1902272
pharmgkbrs1902272
gwascentralrs1902272
openSNPrs1902272
23andMers1902272
23andMe allrs1902272
SNP Nexus

SNPshotrs1902272
SNPdbers1902272
MSV3drs1902272
GWAS Ctlgrs1902272
GMAF0.3365
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 1E-6
Odds Ratio .31 unit increase