SNP Detail For rs8102380
1.Mapping Information
Human SNP ID rs8102380
Human chromosome chr19
Human SNP position 10690509
Pig chromosome chr2
Pig SNP position 69828544
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
Region19p13.2
Chromosome idchr19
Chromosome position10690509
Reported geneILF3
Mapped geneILF3
Upstream gene id
Downstream gene id
SNP gene ids3609
Upstream gene distance
Downstream gene distance
SNP risk allelers8102380-A
SNPsrs8102380
Merged0
SNP id current8102380
Context3_prime_UTR_variant
Intergenic0
Allele frequency0.686
P value0.00000000008
Pvalue mlog10.096910013008
P value text
Or beta0.02
%95 Ci[0.014-0.026] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647