SNP Detail For rs4665058
1.Mapping Information
Human SNP ID rs4665058
Human chromosome chr2
Human SNP position 159333698
Pig chromosome chr15
Pig SNP position 73485426
2.Annotation Information
PubMed ID21738491
JournalPLoS Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21738491
StudyIdentification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.
Disease/TraitSudden cardiac arrest
Initial sample1,283 European ancestry cases, ~20,000 European ancestry controls
Replication sample3,119 European ancestry cases, 11,146 European ancestry controls
Region2q24.2
Chromosome idchr2
Chromosome position159333698
Reported geneBAZ2B
Mapped geneBAZ2B
Upstream gene id
Downstream gene id
SNP gene ids29994
Upstream gene distance
Downstream gene distance
SNP risk allelers4665058-A
SNPsrs4665058
Merged0
SNP id current4665058
Contextintron_variant
Intergenic0
Allele frequency0.014
P value0.0000000002
Pvalue mlog9.69897000433601
P value text
Or beta1.92
%95 Ci[1.57-2.34]
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitsudden cardiac arrest
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004278
Study accessionGCST001132