Human SNP ID | rs1324913 |
---|---|
Human chromosome | chr13 |
Human SNP position | 74061451 |
Pig chromosome | chr11 |
Pig SNP position | 50935367 |
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 | 13q22.1 |
Chromosome id | chr13 |
Chromosome position | 74061451 |
Reported gene | KLF12 |
Mapped gene | KLF12 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 11278 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs1324913-G |
SNPs | rs1324913 |
Merged | 0 |
SNP id current | 1324913 |
Context | regulatory_region_variant |
Intergenic | 0 |
Allele frequency | 0.65 |
P value | 0.0000000003 |
Pvalue mlog | 9.52287874528033 |
P value text | |
Or beta | 0.03 |
%95 Ci | [0.02-0.04] 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 |