Human SNP ID | rs9520462 |
---|---|
Human chromosome | chr13 |
Human SNP position | 107482561 |
Pig chromosome | chr11 |
Pig SNP position | 82460875 |
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 | Reading and spelling |
Initial sample | 6,649 European ancestry children and adolescents |
Replication sample | NA |
Region | 13q33.3 |
Chromosome id | chr13 |
Chromosome position | 107482561 |
Reported gene | FAM155A |
Mapped gene | FAM155A |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 728215 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs9520462-? |
SNPs | rs9520462 |
Merged | 0 |
SNP id current | 9520462 |
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 | reading and spelling ability |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005301 |
Study accession | GCST002062 |