SNP Detail For rs11259936
1.Mapping Information
Human SNP ID rs11259936
Human chromosome chr15
Human SNP position 83911830
Pig chromosome chr7
Pig SNP position 56623183
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
Region15q25.2
Chromosome idchr15
Chromosome position83911830
Reported geneADAMTSL3
Mapped geneADAMTSL3
Upstream gene id
Downstream gene id
SNP gene ids57188
Upstream gene distance
Downstream gene distance
SNP risk allelers11259936-A
SNPsrs11259936
Merged0
SNP id current11259936
Contextintron_variant
Intergenic0
Allele frequency0.48
P value2E-35
Pvalue mlog34.698970004336
P value text
Or beta0.044
%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