Human SNP ID | rs5994434 |
---|---|
Human chromosome | chr22 |
Human SNP position | 31833663 |
Pig chromosome | chr14 |
Pig SNP position | 51748187 |
PubMed ID | 22449649 |
---|---|
Journal | J Am Acad Child Adolesc Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/22449649 |
Study | Genome-wide association study of intelligence: additive effects of novel brain expressed genes. |
Disease/Trait | Intelligence |
Initial sample | 656 European ancestry individuals from ADHD families |
Replication sample | NA |
Region | 22q12.3 |
Chromosome id | chr22 |
Chromosome position | 31833663 |
Reported gene | DEPDC5 |
Mapped gene | DEPDC5 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 9681 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs5994434-? |
SNPs | rs5994434 |
Merged | 0 |
SNP id current | 5994434 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | NR |
P value | 0.0000005 |
Pvalue mlog | 6.30102999566398 |
P value text | (Average Intelligence) |
Or beta | 6.29 |
%95 Ci | [3.88-8.70] unit decrease |
Platform | Illumina [795637] |
CNV | N |
Mapped trait | intelligence |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004337 |
Study accession | GCST001428 |