Human SNP ID | rs3922435 |
---|---|
Human chromosome | chr13 |
Human SNP position | 30740543 |
Pig chromosome | chr11 |
Pig SNP position | 7265069 |
PubMed ID | 23738518 |
---|---|
Journal | Genes Brain Behav |
Link | www.ncbi.nlm.nih.gov/pubmed/23738518 |
Study | A genome-wide association study for reading and language abilities in two population cohorts. |
Disease/Trait | Non-word repetition |
Initial sample | 6,649 European ancestry children and adolescents |
Replication sample | NA |
Region | 13q12.3 |
Chromosome id | chr13 |
Chromosome position | 30740543 |
Reported gene | ALOX5AP |
Mapped gene | ALOX5AP |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 241 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs3922435-? |
SNPs | rs3922435 |
Merged | 0 |
SNP id current | 3922435 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [~ 2400000] (imputed) |
CNV | N |
Mapped trait | non-word reading |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005299 |
Study accession | GCST002059 |