SNP Detail For rs648831
1.Mapping Information
Human SNP ID rs648831
Human chromosome chr6
Human SNP position 80246491
Pig chromosome chr1
Pig SNP position 96519201
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
Region6q14.1
Chromosome idchr6
Chromosome position80246491
Reported geneBCKDHB
Mapped geneBCKDHB
Upstream gene id
Downstream gene id
SNP gene ids594
Upstream gene distance
Downstream gene distance
SNP risk allelers648831-T
SNPsrs648831
Merged0
SNP id current648831
Contextintron_variant
Intergenic0
Allele frequency0.503
P value3E-26
Pvalue mlog25.5228787452803
P value text
Or beta0.031
%95 Ci[0.025-0.037] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647