SNP Detail For rs11677466
1.Mapping Information
Human SNP ID rs11677466
Human chromosome chr2
Human SNP position 232117547
Pig chromosome chr15
Pig SNP position 146520236
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
Region2q37.1
Chromosome idchr2
Chromosome position232117547
Reported geneDIS3L2
Mapped geneDIS3L2
Upstream gene id
Downstream gene id
SNP gene ids129563
Upstream gene distance
Downstream gene distance
SNP risk allelers11677466-A
SNPsrs11677466
Merged0
SNP id current11677466
Contextintron_variant
Intergenic0
Allele frequency0.914
P value3E-23
Pvalue mlog22.5228787452803
P value text
Or beta0.064
%95 Ci[0.05-0.078] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647