Human SNP ID | rs11022756 |
---|---|
Human chromosome | chr11 |
Human SNP position | 13293892 |
Pig chromosome | chr2 |
Pig SNP position | 49394526 |
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 | 11p15.3 |
Chromosome id | chr11 |
Chromosome position | 13293892 |
Reported gene | ARNTL, PTH |
Mapped gene | ARNTL |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 406 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11022756-A |
SNPs | rs11022756 |
Merged | 0 |
SNP id current | 11022756 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.29 |
P value | 7E-20 |
Pvalue mlog | 19.1549019599857 |
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 |