SNP Detail For rs2063730
1.Mapping Information
Human SNP ID rs2063730
Human chromosome chr11
Human SNP position 78337478
Pig chromosome chr9
Pig SNP position 14048733
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
Region11q14.1
Chromosome idchr11
Chromosome position78337478
Reported geneGAB2, THRSP
Mapped geneGAB2
Upstream gene id
Downstream gene id
SNP gene ids9846
Upstream gene distance
Downstream gene distance
SNP risk allelers2063730-C
SNPsrs2063730
Merged0
SNP id current2063730
Contextintron_variant
Intergenic0
Allele frequency0.18
P value0.000000000002
Pvalue mlog11.698970004336
P value text
Or beta0.05
%95 Ci[0.036-0.064] unit increase
PlatformAffymetrix, Illumina [2441815] (imputed)
CNVN
Mapped traitage at menarche
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004703
Study accessionGCST002541