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rs6750634

From SNPedia

Orientationplus
Stabilizedplus
Make rs6750634(A;A)
Make rs6750634(A;G)
Make rs6750634(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position50533365
GeneNRXN1
is asnp
is mentioned by
dbSNPrs6750634
ebirs6750634
HLIrs6750634
Exacrs6750634
Varsomers6750634
Maprs6750634
PheGenIrs6750634
hapmaprs6750634
1000 genomesrs6750634
hgdprs6750634
ensemblrs6750634
gopubmedrs6750634
geneviewrs6750634
scholarrs6750634
googlers6750634
pharmgkbrs6750634
gwascentralrs6750634
openSNPrs6750634
23andMers6750634
23andMe allrs6750634
SNP Nexus

SNPshotrs6750634
SNPdbers6750634
MSV3drs6750634
GWAS Ctlgrs6750634
GMAF0.3815
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 A
P-val 4E-6
Odds Ratio .29 unit decrease