SNP Detail For rs4344931
1.Mapping Information
Human SNP ID rs4344931
Human chromosome chr2
Human SNP position 240879110
Pig chromosome chr15
Pig SNP position 157627409
2.Annotation Information
PubMed ID25282103
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25282103
StudyDefining the role of common variation in the genomic and biological architecture of adult human height.
Disease/TraitHeight
Initial sample253,288 European ancestry individuals
Replication sample80,067 European ancestry individuals
Region2q37.3
Chromosome idchr2
Chromosome position240879110
Reported geneAGXT
Mapped geneAGXT
Upstream gene id
Downstream gene id
SNP gene ids189
Upstream gene distance
Downstream gene distance
SNP risk allelers4344931-A
SNPsrs4344931
Merged0
SNP id current4344931
Context3_prime_UTR_variant
Intergenic0
Allele frequency0.29
P value0.0000000008
Pvalue mlog9.09691001300805
P value text
Or beta0.02
%95 Ci[0.014-0.026] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647