SNP Detail For rs2836950
1.Mapping Information
Human SNP ID rs2836950
Human chromosome chr21
Human SNP position 39232503
Pig chromosome chr13
Pig SNP position 212961110
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
Region21q22.2
Chromosome idchr21
Chromosome position39232503
Reported geneBRWD1
Mapped geneBRWD1
Upstream gene id
Downstream gene id
SNP gene ids54014
Upstream gene distance
Downstream gene distance
SNP risk allelers2836950-C
SNPsrs2836950
Merged0
SNP id current2836950
Contextsplice_region_variant
Intergenic0
Allele frequency0.64
P value0.00000000006
Pvalue mlog10.2218487496163
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