SNP Detail For rs4762767
1.Mapping Information
Human SNP ID rs4762767
Human chromosome chr12
Human SNP position 19713195
Pig chromosome chr5
Pig SNP position 56701697
2.Annotation Information
PubMed ID21946350
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/21946350
StudyGenome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Disease/TraitPulmonary function
Initial sample48,201 European ancestry individuals
Replication sample46,411 European ancestry individuals
Region12p12.3
Chromosome idchr12
Chromosome position19713195
Reported geneAEBP2
Mapped geneLOC101928387 - LOC105369682
Upstream gene id101928387
Downstream gene id105369682
SNP gene ids
Upstream gene distance40106
Downstream gene distance130552
SNP risk allelers4762767-G
SNPsrs4762767
Merged0
SNP id current4762767
Contextintron_variant
Intergenic1
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(FEV1/FVC)
Or beta0.027
%95 Ci[0.015-0.039] unit decrease
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitpulmonary function measurement, FEV/FEC ratio
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003892, http://www.ebi.ac.uk/efo/EFO_0004713
Study accessionGCST001248