Human SNP ID | rs4807927 |
---|---|
Human chromosome | chr19 |
Human SNP position | 1423200 |
Pig chromosome | chr2 |
Pig SNP position | 77951060 |
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 | 19p13.3 |
Chromosome id | chr19 |
Chromosome position | 1423200 |
Reported gene | DAZAP1 |
Mapped gene | DAZAP1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 26528 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4807927-A |
SNPs | rs4807927 |
Merged | 0 |
SNP id current | 4807927 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.94 |
P value | 0.000001 |
Pvalue mlog | 6 |
P value text | |
Or beta | 0.207 |
%95 Ci | [0.12-0.29] unit increase |
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 |
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 | 19p13.3 |
Chromosome id | chr19 |
Chromosome position | 1423200 |
Reported gene | DAZAP1 |
Mapped gene | DAZAP1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 26528 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs4807927-A |
SNPs | rs4807927 |
Merged | 0 |
SNP id current | 4807927 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.94 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
P value text | |
Or beta | 0.147 |
%95 Ci | [0.084-0.21] unit increase |
Platform | Illumina [~ 2400000] (imputed) |
CNV | N |
Mapped trait | word reading |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0005300 |
Study accession | GCST002060 |