SNP Detail For rs1367226
1.Mapping Information
Human SNP ID rs1367226
Human chromosome chr2
Human SNP position 55862405
Pig chromosome chr3
Pig SNP position 90201071
2.Annotation Information
PubMed ID20881960
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/20881960
StudyHundreds of variants clustered in genomic loci and biological pathways affect human height.
Disease/TraitHeight
Initial sample133,653 European ancestry individuals
Replication sample50,074 European ancestry individuals
Region2p16.1
Chromosome idchr2
Chromosome position55862405
Reported geneEFEMP1
Mapped geneLOC105374679
Upstream gene id
Downstream gene id
SNP gene ids105374679
Upstream gene distance
Downstream gene distance
SNP risk allelers1367226-?
SNPsrs1367226
Merged0
SNP id current1367226
Contextdownstream_gene_variant
Intergenic0
Allele frequencyNR
P value0.00000004
Pvalue mlog7.39794000867203
P value text(Conditioned on rs3791675)
Or beta
%95 Ci[NR]
PlatformAffymetrix, Illumina [2834208] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000817