Human SNP ID | rs133885 |
---|---|
Human chromosome | chr22 |
Human SNP position | 25763322 |
Pig chromosome | chr14 |
Pig SNP position | 46293628 |
PubMed ID | 23423138 |
---|---|
Journal | Transl Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/23423138 |
Study | A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. |
Disease/Trait | Mathematical ability in children with dyslexia |
Initial sample | 200 European ancestry cases |
Replication sample | 510 European ancestry cases |
Region | 22q12.1 |
Chromosome id | chr22 |
Chromosome position | 25763322 |
Reported gene | MYO18B |
Mapped gene | MYO18B |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 84700 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs133885-? |
SNPs | rs133885 |
Merged | 0 |
SNP id current | 133885 |
Context | missense_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000000008 |
Pvalue mlog | 9.09691001300805 |
P value text | |
Or beta | 4.87 |
%95 Ci | % increase |
Platform | Illumina [NR] |
CNV | N |
Mapped trait | mathematical ability |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004875 |
Study accession | GCST001866 |