SNP Detail For rs10859567
1.Mapping Information
Human SNP ID rs10859567
Human chromosome chr12
Human SNP position 93733149
Pig chromosome chr5
Pig SNP position 93874851
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
Region12q22
Chromosome idchr12
Chromosome position93733149
Reported geneCRADD
Mapped geneLOC101928731, CRADD
Upstream gene id
Downstream gene id
SNP gene ids101928731, 8738
Upstream gene distance
Downstream gene distance
SNP risk allelers10859567-T
SNPsrs10859567
Merged0
SNP id current10859567
Contextintron_variant
Intergenic0
Allele frequency0.563
P value5E-33
Pvalue mlog32.3010299956639
P value text
Or beta0.035
%95 Ci[0.029-0.041] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647