SNP Detail For rs897080
1.Mapping Information
Human SNP ID rs897080
Human chromosome chr2
Human SNP position 44547063
Pig chromosome chr3
Pig SNP position 101897586
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
Region2p21
Chromosome idchr2
Chromosome position44547063
Reported geneC2orf34
Mapped geneCAMKMT
Upstream gene id
Downstream gene id
SNP gene ids79823
Upstream gene distance
Downstream gene distance
SNP risk allelers897080-T
SNPsrs897080
Merged0
SNP id current897080
Contextintron_variant
Intergenic0
Allele frequency0.743
P value0.0000000000000002
Pvalue mlog15.698970004336
P value text
Or beta0.028
%95 Ci[0.022-0.034] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647