Human SNP ID | rs4083578 |
---|---|
Human chromosome | chr13 |
Human SNP position | 72194571 |
Pig chromosome | chr11 |
Pig SNP position | 48908088 |
PubMed ID | 19734545 |
---|---|
Journal | Hum Mol Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/19734545 |
Study | A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. |
Disease/Trait | Cognitive performance |
Initial sample | Up to 1,295 individuals |
Replication sample | NA |
Region | 13q21.33 |
Chromosome id | chr13 |
Chromosome position | 72194571 |
Reported gene | AL445923.10 |
Mapped gene | DACH1 - RPL21P110 |
Upstream gene id | 1602 |
Downstream gene id | 100271438 |
SNP gene ids | |
Upstream gene distance | 325458 |
Downstream gene distance | 509082 |
SNP risk allele | rs4083578-? |
SNPs | rs4083578 |
Merged | 0 |
SNP id current | 4083578 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.2874 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (SWM strategy) |
Or beta | |
%95 Ci | |
Platform | Illumina [475971] |
CNV | N |
Mapped trait | neuropsychological test |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003926 |
Study accession | GCST000477 |