Rs688034

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is asnp
is mentioned by
dbSNPrs688034
hapmaprs688034
hgdprs688034
ensemblrs688034
gopubmedrs688034
scholarrs688034
googlers688034
pharmgkbrs688034
hgvbaseg2prs688034
medrefsnprs688034
23andMers688034
SNP Nexus

GeneSEZ6L
Chromosome22
Orientationplus
Position25019634
GenotypeEffect
rs688034(T;T)1.6x risk
rs688034(C;T)1.1x risk
rs688034(C;C)normal


Genotypes Magnitude Summary
Rs688034(C;C) 00 normal
Rs688034(C;T) 1.1x risk
Rs688034(T;T) 1.6x risk

rs688034 has been reported in a large study to be associated with heart disease, in particular, coronary artery disease.

The risk allele (oriented to the dbSNP entry) is (T); the odds ratio associated with heterozygotes is 1.11 (CI 0.98-1.25), and for homozygotes, 1.62 (CI 1.34-1.95). [PMID 17554300]

? (C;C) (C;T) (T;T)
GWAS
SNP rs688034
PubMedID [PMID 17554300]
Condition Coronary disease
Gene NR
Risk Allele T
pValue 4.00E-006
OR 1.11
95% CI 0.99-1.25


PharmGKBPA162356656
Name
AnnotationGWAS Results: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls (Initial Sample Size: 1,926 cases, 2,938 controls; Replication Sample Size: (see Samani 2007); Risk Allele: rs688034-T). This variant is associated with coronary disease.
GeneSEZ6L
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesCoronary Disease
Curation LevelNon-Curated