SNP Detail For rs318095
1.Mapping Information
Human SNP ID rs318095
Human chromosome chr17
Human SNP position 48897372
Pig chromosome chr12
Pig SNP position 25070279
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
Region17q21.32
Chromosome idchr17
Chromosome position48897372
Reported geneATP5G1
Mapped geneATP5G1 - UBE2Z
Upstream gene id516
Downstream gene id65264
SNP gene ids
Upstream gene distance1501
Downstream gene distance10997
SNP risk allelers318095-T
SNPsrs318095
Merged0
SNP id current318095
Contextintron_variant
Intergenic1
Allele frequency0.463
P value0.0000000000000002
Pvalue mlog15.698970004336
P value text
Or beta0.024
%95 Ci[0.018-0.03] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647