SNP Detail For rs2074977
1.Mapping Information
Human SNP ID rs2074977
Human chromosome chr19
Human SNP position 3434030
Pig chromosome chr2
Pig SNP position 75690767
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
Region19p13.3
Chromosome idchr19
Chromosome position3434030
Reported geneNFIC
Mapped geneNFIC
Upstream gene id
Downstream gene id
SNP gene ids4782
Upstream gene distance
Downstream gene distance
SNP risk allelers2074977-A
SNPsrs2074977
Merged0
SNP id current2074977
Contextintron_variant
Intergenic0
Allele frequency0.637
P value2E-20
Pvalue mlog19.698970004336
P value text
Or beta0.029
%95 Ci[0.023-0.035] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647