SNP Detail For rs7926971
1.Mapping Information
Human SNP ID rs7926971
Human chromosome chr11
Human SNP position 12676493
Pig chromosome chr2
Pig SNP position 50099327
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
Region11p15.3
Chromosome idchr11
Chromosome position12676493
Reported geneTEAD1
Mapped geneTEAD1
Upstream gene id
Downstream gene id
SNP gene ids7003
Upstream gene distance
Downstream gene distance
SNP risk allelers7926971-A
SNPsrs7926971
Merged0
SNP id current7926971
Contextintron_variant
Intergenic0
Allele frequency0.55
P value0.0000000004
Pvalue mlog9.39794000867203
P value text
Or beta0.023
%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