SNP Detail For rs11465699
1.Mapping Information
Human SNP ID rs11465699
Human chromosome chr2
Human SNP position 102438307
Pig chromosome chr3
Pig SNP position 54257787
2.Annotation Information
PubMed ID23999434
JournalJ Clin Invest
Linkwww.ncbi.nlm.nih.gov/pubmed/23999434
StudyCommon genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.
Disease/TraitSerum protein levels (sST2)
Initial sample2,797 individuals
Replication sampleNA
Region2q12.1
Chromosome idchr2
Chromosome position102438307
Reported geneIL18RAP
Mapped geneIL18RAP
Upstream gene id
Downstream gene id
SNP gene ids8807
Upstream gene distance
Downstream gene distance
SNP risk allelers11465699-A
SNPsrs11465699
Merged0
SNP id current11465699
Contextintron_variant
Intergenic0
Allele frequency0.06
P value0.00000002
Pvalue mlog7.69897000433601
P value text
Or beta0.14
%95 Ci[0.1-0.18] unit increase
PlatformAffymetrix [2500000] (imputed)
CNVN
Mapped traitserum ST2 measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005416
Study accessionGCST002166