SNP Detail For rs1324913
1.Mapping Information
Human SNP ID rs1324913
Human chromosome chr13
Human SNP position 74061451
Pig chromosome chr11
Pig SNP position 50935367
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
Region13q22.1
Chromosome idchr13
Chromosome position74061451
Reported geneKLF12
Mapped geneKLF12
Upstream gene id
Downstream gene id
SNP gene ids11278
Upstream gene distance
Downstream gene distance
SNP risk allelers1324913-G
SNPsrs1324913
Merged0
SNP id current1324913
Contextregulatory_region_variant
Intergenic0
Allele frequency0.65
P value0.0000000003
Pvalue mlog9.52287874528033
P value text
Or beta0.03
%95 Ci[0.02-0.04] unit increase
PlatformAffymetrix, Illumina [2441815] (imputed)
CNVN
Mapped traitage at menarche
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004703
Study accessionGCST002541