SNP Detail For rs9844666
1.Mapping Information
Human SNP ID rs9844666
Human chromosome chr3
Human SNP position 136255374
Pig chromosome chr13
Pig SNP position 84590930
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
Region3q22.3
Chromosome idchr3
Chromosome position136255374
Reported genePCCB
Mapped genePCCB
Upstream gene id
Downstream gene id
SNP gene ids5096
Upstream gene distance
Downstream gene distance
SNP risk allelers9844666-A
SNPsrs9844666
Merged0
SNP id current9844666
Context5_prime_UTR_variant
Intergenic0
Allele frequency0.25
P value0.000000004
Pvalue mlog8.39794000867203
P value text
Or beta0.024
%95 Ci[NR] unit decrease
PlatformAffymetrix, Illumina [2834208] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000817