Rs8055236

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is asnp
is mentioned by
dbSNPrs8055236
hapmaprs8055236
hgdprs8055236
ensemblrs8055236
gopubmedrs8055236
scholarrs8055236
googlers8055236
pharmgkbrs8055236
hgvbaseg2prs8055236
medrefsnprs8055236
23andMers8055236
SNP Nexus

GeneCDH13
Chromosome16
Orientationplus
Position81769898
GenotypeEffect
rs8055236(G;G)2.2x risk
rs8055236(G;T)1.9x risk
rs8055236(T;T)normal


Genotypes Magnitude Summary
Rs8055236(A;A) 00
Rs8055236(G;G)
Rs8055236(G;T) 1.9x risk
Rs8055236(T;T) 00 normal

rs8055236 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 (G); the odds ratio associated with heterozygotes is 1.91 (CI 1.33-2.74), and for homozygotes, 2.23 (CI 1.56-3.17). [PMID 17554300]

? (G;G) (G;T) (T;T)
GWAS
SNP rs8055236
PubMedID [PMID 17554300]
Condition Coronary disease
Gene NR
Risk Allele G
pValue 6.00E-006
OR 1.91
95% CI 1.33-2.74


PharmGKBPA162356658
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: rs8055236-G). This variant is associated with coronary disease.
GeneCDH13
Featue
EvidencePubMed ID:17554300; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesCoronary Disease
Curation LevelNon-Curated