Rs2943634

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is asnp
is mentioned by
dbSNPrs2943634
hapmaprs2943634
hgdprs2943634
ensemblrs2943634
gopubmedrs2943634
scholarrs2943634
googlers2943634
pharmgkbrs2943634
hgvbaseg2prs2943634
medrefsnprs2943634
23andMers2943634
SNP Nexus

Chromosome2
Orientationplus
Position226776323
GenotypeEffect
rs2943634(A;A)*?
rs2943634(A;C)*?
rs2943634(C;C)*?


rs2943634 is a SNP found to be reproducibly associated with heart disease [PMID 17634449] [PMID 18979498] rs2943634 associated with high density lipoprotein (HDL) cholesterol

GWAS
SNP rs2943634
PubMedID [PMID 17634449]
Condition Coronary disease
Gene pseudogene
Risk Allele C
pValue 2.00E-007
OR 1.21
95% CI 1.13-1.30


[PMID 19164808] Large scale association analysis of novel genetic loci for coronary artery disease


[PMID 18675980] Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes

PharmGKBPA162356674
Name
AnnotationGWAS Results: Genomewide association analysis of coronary artery disease (Initial Sample Size: 1,926 cases, 2,938 controls; Replication Sample Size: 875 cases, 1,644 controls; Risk Allele: rs2943634-C).
Gene-
Featue
EvidencePubMed ID:17634449; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesCoronary Disease
Curation LevelNon-Curated
? (A;A) (A;C) (C;C)