Rs683395

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is asnp
is mentioned by
dbSNPrs683395
hapmaprs683395
hgdprs683395
ensemblrs683395
gopubmedrs683395
scholarrs683395
googlers683395
pharmgkbrs683395
hgvbaseg2prs683395
medrefsnprs683395
23andMers683395
SNP Nexus

GeneLAMP3
Chromosome3
Orientationminus
Position184352511
GenotypeEffect
rs683395(C;C)1.3x risk
rs683395(C;T)1.5x risk
rs683395(T;T)normal


Genotypes Magnitude Summary
Rs683395(A;A) 00
Rs683395(C;C) 1.3x risk
Rs683395(C;T) 1.5x risk
Rs683395(T;T) 00 normal

rs683395 has been reported in a large study to be associated with bipolar disorder.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.47 (CI 1.26-1.71), and for homozygotes, 1.3 (CI 0.69-2.46). [PMID 17554300]

? (C;C) (C;T) (T;T)
GWAS
SNP rs683395
PubMedID [PMID 17554300]
Condition Bipolar disorder
Gene NR
Risk Allele G
pValue 5.00E-006
OR 1.47
95% CI 1.26-1.71


PharmGKBPA162356655
Name
AnnotationGWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,868 cases, 2,938 controls; Replication Sample Size: NR; Risk Allele: rs683395-G). This variant is associated with bipolar disorder.
GeneLAMP3
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesBipolar Disorder
Curation LevelNon-Curated