SNP Detail For rs11022756
1.Mapping Information
Human SNP ID rs11022756
Human chromosome chr11
Human SNP position 13293892
Pig chromosome chr2
Pig SNP position 49394526
2.Annotation Information
PubMed ID25231870
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/25231870
StudyParent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
Disease/TraitMenarche (age at onset)
Initial sampleUp to 182,413 European ancestry females
Replication sampleNA
Region11p15.3
Chromosome idchr11
Chromosome position13293892
Reported geneARNTL, PTH
Mapped geneARNTL
Upstream gene id
Downstream gene id
SNP gene ids406
Upstream gene distance
Downstream gene distance
SNP risk allelers11022756-A
SNPsrs11022756
Merged0
SNP id current11022756
Contextintron_variant
Intergenic0
Allele frequency0.29
P value7E-20
Pvalue mlog19.1549019599857
P value text
Or beta0.05
%95 Ci[0.038-0.062] unit increase
PlatformAffymetrix, Illumina [2441815] (imputed)
CNVN
Mapped traitage at menarche
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004703
Study accessionGCST002541