SNP Detail For rs3739707
1.Mapping Information
Human SNP ID rs3739707
Human chromosome chr9
Human SNP position 111030426
Pig chromosome chr1
Pig SNP position 282802399
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
Region9q31.3
Chromosome idchr9
Chromosome position111030426
Reported geneLPAR1
Mapped geneLPAR1
Upstream gene id
Downstream gene id
SNP gene ids1902
Upstream gene distance
Downstream gene distance
SNP risk allelers3739707-A
SNPsrs3739707
Merged0
SNP id current3739707
Contextintron_variant
Intergenic0
Allele frequency0.247
P value0.000000000004
Pvalue mlog11.397940008672
P value text
Or beta0.024
%95 Ci[0.016-0.032] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647