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rs6765687

From SNPedia

Orientationplus
Stabilizedplus
Make rs6765687(C;C)
Make rs6765687(C;T)
Make rs6765687(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position52699090
GeneGLT8D1
is asnp
is mentioned by
dbSNPrs6765687
ebirs6765687
HLIrs6765687
Exacrs6765687
Varsomers6765687
Maprs6765687
PheGenIrs6765687
hapmaprs6765687
1000 genomesrs6765687
hgdprs6765687
ensemblrs6765687
gopubmedrs6765687
geneviewrs6765687
scholarrs6765687
googlers6765687
pharmgkbrs6765687
gwascentralrs6765687
openSNPrs6765687
23andMers6765687
23andMe allrs6765687
SNP Nexus

SNPshotrs6765687
SNPdbers6765687
MSV3drs6765687
GWAS Ctlgrs6765687
GMAF0.1928
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23453885OA-icon.png]
Trait Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele T
P-val 5E-6
Odds Ratio 1.07 [1.04-1.11]