SNP Detail For rs2687950
1.Mapping Information
Human SNP ID rs2687950
Human chromosome chr13
Human SNP position 50144332
Pig chromosome chr11
Pig SNP position 18005258
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
Region13q14.2
Chromosome idchr13
Chromosome position50144332
Reported geneKCNRG
Mapped geneDLEU1
Upstream gene id
Downstream gene id
SNP gene ids10301
Upstream gene distance
Downstream gene distance
SNP risk allelers2687950-T
SNPsrs2687950
Merged0
SNP id current2687950
Contextintron_variant
Intergenic0
Allele frequency0.254
P value9E-27
Pvalue mlog26.0457574905606
P value text
Or beta0.036
%95 Ci[0.03-0.042] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647