SNP Detail For rs711245
1.Mapping Information
Human SNP ID rs711245
Human chromosome chr2
Human SNP position 36541732
Pig chromosome chr3
Pig SNP position 110268153
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
Region2p22.2
Chromosome idchr2
Chromosome position36541732
Reported geneCRIM1
Mapped geneCRIM1
Upstream gene id
Downstream gene id
SNP gene ids51232
Upstream gene distance
Downstream gene distance
SNP risk allelers711245-A
SNPsrs711245
Merged0
SNP id current711245
Contextintron_variant
Intergenic0
Allele frequency0.332
P value0.00000000000004
Pvalue mlog13.397940008672
P value text
Or beta0.024
%95 Ci[0.018-0.03] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647