Human SNP ID | rs11577628 |
---|---|
Human chromosome | chr1 |
Human SNP position | 162349734 |
Pig chromosome | chr4 |
Pig SNP position | 95875500 |
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 | Word reading |
Initial sample | 6,649 European ancestry children and adolescents |
Replication sample | |
Region | 1q23.3 |
Chromosome id | chr1 |
Chromosome position | 162349734 |
Reported gene | NOS1AP |
Mapped gene | NOS1AP |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9722 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11577628-A |
SNPs | rs11577628 |
Merged | 0 |
SNP id current | 11577628 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.92 |
P value | 0.000005 |
Pvalue mlog | 5.30102999566398 |
P value text | |
Or beta | 0.123 |
%95 Ci | [0.07-0.176] unit decrease |
Platform | Illumina [~ 2400000] (imputed) |
CNV | N |
Mapped trait | word reading |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005300 |
Study accession | GCST002060 |