SNP Detail For rs11000019
1.Mapping Information
Human SNP ID rs11000019
Human chromosome chr10
Human SNP position 71831773
Pig chromosome chr14
Pig SNP position 80638770
2.Annotation Information
PubMed ID23829686
JournalHum Genomics
Linkwww.ncbi.nlm.nih.gov/pubmed/23829686
StudyRank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.
Disease/TraitAsthma (childhood onset)
Initial sample429 European ancestry affected offspring trios
Replication sample52 African American affected offspring trios, 46 Hispanic affected offspring trios
Region10q22.1
Chromosome idchr10
Chromosome position71831773
Reported genePSAP
Mapped genePSAP
Upstream gene id
Downstream gene id
SNP gene ids5660
Upstream gene distance
Downstream gene distance
SNP risk allelers11000019-?
SNPsrs11000019
Merged0
SNP id current11000019
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.00000008
Pvalue mlog7.09691001300805
P value text
Or beta
%95 Ci
PlatformAffymetrix [786195]
CNVN
Mapped traitchildhood onset asthma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004591
Study accessionGCST002088