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rs7069733

From SNPedia

Orientationplus
Stabilizedplus
Make rs7069733(C;C)
Make rs7069733(C;G)
Make rs7069733(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position103538013
GeneNEURL
is asnp
is mentioned by
dbSNPrs7069733
ebirs7069733
HLIrs7069733
Exacrs7069733
Varsomers7069733
Maprs7069733
PheGenIrs7069733
hapmaprs7069733
1000 genomesrs7069733
hgdprs7069733
ensemblrs7069733
gopubmedrs7069733
geneviewrs7069733
scholarrs7069733
googlers7069733
pharmgkbrs7069733
gwascentralrs7069733
openSNPrs7069733
23andMers7069733
23andMe allrs7069733
SNP Nexus

SNPshotrs7069733
SNPdbers7069733
MSV3drs7069733
GWAS Ctlgrs7069733
GMAF0.2227
Max Magnitude
? (C;C) (C;G) (G;G) 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 C
P-val 7E-6
Odds Ratio 1.08 [1.04-1.12]