SNP Detail For rs9969804
1.Mapping Information
Human SNP ID rs9969804
Human chromosome chr9
Human SNP position 92666838
Pig chromosome chr3
Pig SNP position 43599709
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
Region9q22.31
Chromosome idchr9
Chromosome position92666838
Reported geneIPPK
Mapped geneIPPK
Upstream gene id
Downstream gene id
SNP gene ids64768
Upstream gene distance
Downstream gene distance
SNP risk allelers9969804-A
SNPsrs9969804
Merged0
SNP id current9969804
Contextintron_variant
Intergenic0
Allele frequency0.44
P value0.00000000000000008
Pvalue mlog16.096910013008
P value text
Or beta0.03
%95 Ci[NR] unit increase
PlatformAffymetrix, Illumina [2834208] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000817