Rs10033464

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dbSNPrs10033464
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hgdprs10033464
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hgvbaseg2prs10033464
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23andMers10033464
SNP Nexus

Chromosome4
Orientationplus
Position111940209
GenotypeEffect
rs10033464(G;G)1.4x increased risk of atrial fibrillation and ischemic stroke
rs10033464(G;T)1.4x increased risk of atrial fibrillation and ischemic stroke
rs10033464(T;T)normal


Genotypes Magnitude Summary
Rs10033464(G;G) 1.4x increased risk of atrial fibrillation and ischemic stroke
Rs10033464(G;T) 1.4x increased risk of atrial fibrillation and ischemic stroke
Rs10033464(T;T) normal
Two SNPs from chromosome 4q25, rs2200733 and rs10033464, were found to be associated with atrial fibrillation in a study of both European and Asian populations. The odds ratio associated with one or more copies of either risk allele was ~1.4x.[PMID 17603472]

[PMID 18991354] In 1,661 Icelandic ischemic stroke samples and two large European replication sets combined, rs10033464 was associated with cardioembolic stroke (CES) (odds ratio 1.27, p = 6.1 x 10e-4).

[PMID 19141561] rs2200733 and rs10033464 are strongly associated with AF in four cohorts of European descent.

? (G;G) (G;T) (T;T)
GWAS
SNP rs10033464
PubMedID [PMID 17603472]
Condition Atrial fibrillation/atrial flutter
Gene PITX2,ENPEP
Risk Allele T
pValue 7.00E-011
OR 1.39
95% CI 1.26-1.53


Related to ATRIAL FIBRILLATION, FAMILIAL, 5; ATFB5 according to omim 611494. See also


PharmGKBPA162356664
Name
AnnotationGWAS Results: Variants conferring risk of atrial fibrillation on chromosome 4q25 (Initial Sample Size: 550 cases, 4,476 controls; Replication Sample Size: 3,363 cases, 17,616 controls; Risk Allele: rs10033464-T). This variant is associated with atrial fibrillation and atrial flutter.
Gene-
Featue
EvidencePubMed ID:17603472; Web Resource:http://www.genome.gov/gwastudies/
Drugs
DiseasesAtrial Fibrillation, Atrial Flutter
Curation LevelNon-Curated