SNP Detail For rs6920372
1.Mapping Information
Human SNP ID rs6920372
Human chromosome chr6
Human SNP position 109402736
Pig chromosome chr16
Pig SNP position 28242252
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
Region6q21
Chromosome idchr6
Chromosome position109402736
Reported genePPIL6
Mapped genePPIL6
Upstream gene id
Downstream gene id
SNP gene ids285755
Upstream gene distance
Downstream gene distance
SNP risk allelers6920372-A
SNPsrs6920372
Merged0
SNP id current6920372
Contextintron_variant
Intergenic0
Allele frequency0.413
P value0.00000000000000002
Pvalue mlog16.698970004336
P value text
Or beta0.025
%95 Ci[0.019-0.031] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647