SNP Detail For rs4756059
1.Mapping Information
Human SNP ID rs4756059
Human chromosome chr11
Human SNP position 46129068
Pig chromosome chr2
Pig SNP position 17681356
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
Region11p11.2
Chromosome idchr11
Chromosome position46129068
Reported genePHF21A
Mapped geneLOC105376661
Upstream gene id
Downstream gene id
SNP gene ids105376661
Upstream gene distance
Downstream gene distance
SNP risk allelers4756059-T
SNPsrs4756059
Merged0
SNP id current4756059
Contextintron_variant
Intergenic0
Allele frequency0.92
P value0.0000000000005
Pvalue mlog12.3010299956639
P value text
Or beta0.07
%95 Ci[0.05-0.09] unit increase
PlatformAffymetrix, Illumina [2441815] (imputed)
CNVN
Mapped traitage at menarche
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004703
Study accessionGCST002541