SNP Detail For rs2289195
1.Mapping Information
Human SNP ID rs2289195
Human chromosome chr2
Human SNP position 25240614
Pig chromosome chr3
Pig SNP position 120652185
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
Region2p23.3
Chromosome idchr2
Chromosome position25240614
Reported geneDNMT3A
Mapped geneDNMT3A
Upstream gene id
Downstream gene id
SNP gene ids1788
Upstream gene distance
Downstream gene distance
SNP risk allelers2289195-A
SNPsrs2289195
Merged0
SNP id current2289195
Contextintron_variant
Intergenic0
Allele frequency0.43
P value2E-37
Pvalue mlog36.698970004336
P value text
Or beta0.038
%95 Ci[0.032-0.044] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647