Human SNP ID | rs7647973 |
---|---|
Human chromosome | chr3 |
Human SNP position | 49473498 |
Pig chromosome | JH118489-1 |
Pig SNP position | 59743 |
PubMed ID | 25231870 |
---|---|
Journal | Nature |
Link | www.ncbi.nlm.nih.gov/pubmed/25231870 |
Study | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. |
Disease/Trait | Menarche (age at onset) |
Initial sample | Up to 182,413 European ancestry females |
Replication sample | NA |
Region | 3p21.31 |
Chromosome id | chr3 |
Chromosome position | 49473498 |
Reported gene | WDR6, UBA7 |
Mapped gene | DAG1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 1605 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7647973-A |
SNPs | rs7647973 |
Merged | 0 |
SNP id current | 7647973 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.26 |
P value | 0.0000000000000001 |
Pvalue mlog | 16 |
P value text | |
Or beta | 0.05 |
%95 Ci | [0.038-0.062] unit increase |
Platform | Affymetrix, Illumina [2441815] (imputed) |
CNV | N |
Mapped trait | age at menarche |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004703 |
Study accession | GCST002541 |