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rs4650608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 0 common in complete genomics
Make rs4650608(C;C)
Make rs4650608(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position78772330
is asnp
is mentioned by
dbSNPrs4650608
ebirs4650608
HLIrs4650608
Exacrs4650608
Varsomers4650608
Maprs4650608
PheGenIrs4650608
hapmaprs4650608
1000 genomesrs4650608
hgdprs4650608
ensemblrs4650608
gopubmedrs4650608
geneviewrs4650608
scholarrs4650608
googlers4650608
pharmgkbrs4650608
gwascentralrs4650608
openSNPrs4650608
23andMers4650608
23andMe allrs4650608
SNP Nexus

SNPshotrs4650608
SNPdbers4650608
MSV3drs4650608
GWAS Ctlgrs4650608
GMAF0.2291
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22182935]
Trait
Title Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.
Risk Allele T
P-val 0.000001
Odds Ratio None None
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 1E-6
Odds Ratio 1.06 [1.03-1.09]
GWAS snp
PMID [PMID 24280982OA-icon.png]
Trait Schizophrenia or bipolar disorder
Title Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.
Risk Allele
P-val 8E-9
Odds Ratio NR NR