SNP Detail For rs10765792
1.Mapping Information
Human SNP ID rs10765792
Human chromosome chr11
Human SNP position 96133536
Pig chromosome chr9
Pig SNP position 32189270
2.Annotation Information
PubMed ID21658281
JournalBMC Cardiovasc Disord
Linkwww.ncbi.nlm.nih.gov/pubmed/21658281
StudyGWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
Disease/TraitSudden cardiac arrest
Initial sample88 European ancestry cases, 517 European ancestry controls
Replication sampleNA
Region11q21
Chromosome idchr11
Chromosome position96133536
Reported geneintergenic
Mapped geneMAML2
Upstream gene id
Downstream gene id
SNP gene ids84441
Upstream gene distance
Downstream gene distance
SNP risk allelers10765792-?
SNPsrs10765792
Merged0
SNP id current10765792
Contextintron_variant
Intergenic0
Allele frequency0.11
P value0.0000000000008
Pvalue mlog12.096910013008
P value text(Recessive)
Or beta1.54
%95 Ci[1.37-1.72]
PlatformAffymetrix [319222]
CNVN
Mapped traitsudden cardiac arrest
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004278
Study accessionGCST001099