SNP Detail For rs4673659
1.Mapping Information
Human SNP ID rs4673659
Human chromosome chr2
Human SNP position 212325005
Pig chromosome chr15
Pig SNP position 126853876
2.Annotation Information
PubMed ID24824216
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/24824216
StudyGenome-wide interaction studies reveal sex-specific asthma risk alleles.
Disease/TraitAsthma (sex interaction)
Initial sample1,052 European ancestry male cases, 1,019 European ancestry female cases, 709 European ancestry male controls, 826 European ancestry female controls, 675 African American/African Caribbean male cases, 837 African American/African Caribbean female cases, 5
Replication sampleNA
Region2q34
Chromosome idchr2
Chromosome position212325005
Reported geneERBB4
Mapped geneERBB4
Upstream gene id
Downstream gene id
SNP gene ids2066
Upstream gene distance
Downstream gene distance
SNP risk allelers4673659-C
SNPsrs4673659
Merged0
SNP id current4673659
Contextintron_variant
Intergenic0
Allele frequency0.72
P value0.0000009
Pvalue mlog6.04575749056067
P value text(Latino, female)
Or beta1.42
%95 Ci[1.23-1.64]
PlatformAffymetrix, Illumina [~ 2100000] (imputed)
CNVN
Mapped traitasthma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000270
Study accessionGCST002445