SNP Detail For rs994533
1.Mapping Information
Human SNP ID rs994533
Human chromosome chr2
Human SNP position 217419555
Pig chromosome chr15
Pig SNP position 132574576
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
Region2q35
Chromosome idchr2
Chromosome position217419555
Reported geneTNS1
Mapped geneDIRC3
Upstream gene id
Downstream gene id
SNP gene ids729582
Upstream gene distance
Downstream gene distance
SNP risk allelers994533-C
SNPsrs994533
Merged0
SNP id current994533
Contextintron_variant
Intergenic0
Allele frequency0.331
P value0.00000000000000001
Pvalue mlog17
P value text
Or beta0.027
%95 Ci[0.021-0.033] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647