SNP Detail For rs16929097
1.Mapping Information
Human SNP ID rs16929097
Human chromosome chr9
Human SNP position 12521826
Pig chromosome chr1
Pig SNP position 233857275
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
Region9p23
Chromosome idchr9
Chromosome position12521826
Reported geneintergenic
Mapped geneLOC105375976 - TYRP1
Upstream gene id105375976
Downstream gene id7306
SNP gene ids
Upstream gene distance362711
Downstream gene distance171560
SNP risk allelers16929097-?
SNPsrs16929097
Merged0
SNP id current16929097
Contextintergenic_variant
Intergenic1
Allele frequencyNR
P value0.000000008
Pvalue mlog8.09691001300805
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