SNP Detail For rs2279008
1.Mapping Information
Human SNP ID rs2279008
Human chromosome chr19
Human SNP position 17172493
Pig chromosome chr2
Pig SNP position 60053375
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
Region19p13.11
Chromosome idchr19
Chromosome position17172493
Reported geneMYO9B
Mapped geneMYO9B
Upstream gene id
Downstream gene id
SNP gene ids4650
Upstream gene distance
Downstream gene distance
SNP risk allelers2279008-T
SNPsrs2279008
Merged0
SNP id current2279008
Contextintron_variant
Intergenic0
Allele frequency0.74
P value0.00000003
Pvalue mlog7.52287874528033
P value text
Or beta0.025
%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