SNP Detail For rs4884502
1.Mapping Information
Human SNP ID rs4884502
Human chromosome chr13
Human SNP position 63636265
Pig chromosome chr11
Pig SNP position 38633655
2.Annotation Information
PubMed ID24792382
JournalClin Chim Acta
Linkwww.ncbi.nlm.nih.gov/pubmed/24792382
StudyGenome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid.
Disease/TraitResponse to inhaled corticosteroid treatment in asthma (percentage change of FEV1)
Initial sample189 Korean ancestry cases
Replication sampleNA
Region13q21.31
Chromosome idchr13
Chromosome position63636265
Reported geneOR7E156P
Mapped geneLOC105370236
Upstream gene id
Downstream gene id
SNP gene ids105370236
Upstream gene distance
Downstream gene distance
SNP risk allelers4884502-?
SNPsrs4884502
Merged0
SNP id current4884502
Contextregulatory_region_variant
Intergenic0
Allele frequency
P value0.000009
Pvalue mlog5.04575749056067
P value text
Or beta0.32
%95 Ci[NR] unit increase
PlatformIllumina [430487]
CNVN
Mapped traitFEV change measurement, response to corticosteroid, asthma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0000270
Study accessionGCST002432