Human SNP ID | rs4839516 |
---|---|
Human chromosome | chr1 |
Human SNP position | 116197828 |
Pig chromosome | chr4 |
Pig SNP position | 114640742 |
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 | 1p13.1 |
Chromosome id | chr1 |
Chromosome position | 116197828 |
Reported gene | intergenic |
Mapped gene | MAB21L3 - LOC105378919 |
Upstream gene id | 126868 |
Downstream gene id | 105378919 |
SNP gene ids | |
Upstream gene distance | 62588 |
Downstream gene distance | 43136 |
SNP risk allele | rs4839516-A |
SNPs | rs4839516 |
Merged | 0 |
SNP id current | 4839516 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.31 |
P value | 0.0000004 |
Pvalue mlog | 6.39794000867203 |
P value text | |
Or beta | 0.079 |
%95 Ci | [0.05-0.108] 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 |