SNP Detail For rs8007661
1.Mapping Information
Human SNP ID rs8007661
Human chromosome chr14
Human SNP position 91993614
Pig chromosome chr7
Pig SNP position 120157080
2.Annotation Information
PubMed ID18391950
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/18391950
StudyIdentification of ten loci associated with height highlights new biological pathways in human growth.
Disease/TraitHeight
Initial sample15,821 European ancestry individuals
Replication sampleUp to 17,801 European ancestry individuals
Region14q32.12
Chromosome idchr14
Chromosome position91993614
Reported geneTRIP11, ATXN3
Mapped geneTRIP11
Upstream gene id
Downstream gene id
SNP gene ids9321
Upstream gene distance
Downstream gene distance
SNP risk allelers8007661-T
SNPsrs8007661
Merged0
SNP id current8007661
Contextintron_variant
Intergenic0
Allele frequency0.3
P value0.0000000006
Pvalue mlog9.22184874961635
P value text
Or beta0.42
%95 Ci[0.30-0.54] cm decrease
PlatformAffymetrix, Illumina [2260683] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000176