SNP Detail For rs9475752
1.Mapping Information
Human SNP ID rs9475752
Human chromosome chr6
Human SNP position 56915943
Pig chromosome chr7
Pig SNP position 33312158
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
Region6p12.1
Chromosome idchr6
Chromosome position56915943
Reported geneDST, BEND6
Mapped geneDST
Upstream gene id
Downstream gene id
SNP gene ids667
Upstream gene distance
Downstream gene distance
SNP risk allelers9475752-C
SNPsrs9475752
Merged0
SNP id current9475752
Contextintron_variant
Intergenic0
Allele frequency0.81
P value0.000000000008
Pvalue mlog11.096910013008
P value text
Or beta0.04
%95 Ci[0.028-0.052] unit increase
PlatformAffymetrix, Illumina [2441815] (imputed)
CNVN
Mapped traitage at menarche
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004703
Study accessionGCST002541