SNP Detail For rs4711336
1.Mapping Information
Human SNP ID rs4711336
Human chromosome chr6
Human SNP position 33691269
Pig chromosome chr7
Pig SNP position 34504450
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
Region6p21.31
Chromosome idchr6
Chromosome position33691269
Reported geneHMGA1
Mapped geneITPR3
Upstream gene id
Downstream gene id
SNP gene ids3710
Upstream gene distance
Downstream gene distance
SNP risk allelers4711336-?
SNPsrs4711336
Merged0
SNP id current4711336
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.00000003
Pvalue mlog7.52287874528033
P value text(Conditiond on rs2780226)
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