SNP Detail For rs4620037
1.Mapping Information
Human SNP ID rs4620037
Human chromosome chr5
Human SNP position 171448093
Pig chromosome chr16
Pig SNP position 56930349
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
Region5q35.1
Chromosome idchr5
Chromosome position171448093
Reported geneFGF18
Mapped geneFGF18, LOC105377719
Upstream gene id
Downstream gene id
SNP gene ids8817, 105377719
Upstream gene distance
Downstream gene distance
SNP risk allelers4620037-A
SNPsrs4620037
Merged0
SNP id current4620037
Contextintron_variant
Intergenic0
Allele frequency0.796
P value0.000000000000000001
Pvalue mlog18
P value text
Or beta0.032
%95 Ci[0.024-0.04] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647