SNP Detail For rs301901
1.Mapping Information
Human SNP ID rs301901
Human chromosome chr5
Human SNP position 37046524
Pig chromosome chr16
Pig SNP position 23494905
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
Region5p13.2
Chromosome idchr5
Chromosome position37046524
Reported geneNIPBL
Mapped geneNIPBL
Upstream gene id
Downstream gene id
SNP gene ids25836
Upstream gene distance
Downstream gene distance
SNP risk allelers301901-A
SNPsrs301901
Merged0
SNP id current301901
Contextintron_variant
Intergenic0
Allele frequency0.565
P value0.0000000000000004
Pvalue mlog15.397940008672
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