SNP Detail For rs2341459
1.Mapping Information
Human SNP ID rs2341459
Human chromosome chr2
Human SNP position 44541063
Pig chromosome chr3
Pig SNP position 101903523
2.Annotation Information
PubMed ID20881960
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/20881960
StudyHundreds of variants clustered in genomic loci and biological pathways affect human height.
Disease/TraitHeight
Initial sample133,653 European ancestry individuals
Replication sample50,074 European ancestry individuals
Region2p21
Chromosome idchr2
Chromosome position44541063
Reported geneC2orf34
Mapped geneCAMKMT
Upstream gene id
Downstream gene id
SNP gene ids79823
Upstream gene distance
Downstream gene distance
SNP risk allelers2341459-T
SNPsrs2341459
Merged0
SNP id current2341459
Contextintron_variant
Intergenic0
Allele frequency0.27
P value0.0000000008
Pvalue mlog9.09691001300805
P value text
Or beta0.025
%95 Ci[NR] unit increase
PlatformAffymetrix, Illumina [2834208] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000817