SNP Detail For rs2274432
1.Mapping Information
Human SNP ID rs2274432
Human chromosome chr1
Human SNP position 184051811
Pig chromosome chr9
Pig SNP position 137621761
2.Annotation Information
PubMed ID18391951
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/18391951
StudyMany sequence variants affecting diversity of adult human height.
Disease/TraitHeight
Initial sample30,968 European ancestry individuals
Replication sample8,541 European ancestry individuals
Region1q25.3
Chromosome idchr1
Chromosome position184051811
Reported geneGLT25D2, C1orf19
Mapped geneTSEN15
Upstream gene id
Downstream gene id
SNP gene ids116461
Upstream gene distance
Downstream gene distance
SNP risk allelers2274432-T
SNPsrs2274432
Merged0
SNP id current2274432
Contextmissense_variant
Intergenic0
Allele frequency0.37
P value0.000000008
Pvalue mlog8.09691001300805
P value text
Or beta5.3
%95 Ci[3.54-7.06] % s.d. increase
PlatformAffymetrix, Illumina [up to 304226]
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000175