Human SNP ID | rs13113376 |
---|---|
Human chromosome | chr4 |
Human SNP position | 130211745 |
Pig chromosome | chr8 |
Pig SNP position | 101519083 |
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 | 4q28.3 |
Chromosome id | chr4;4;4;4 |
Chromosome position | 130210261;130211745;130206478;130212336 |
Reported gene | CYCSP14 |
Mapped gene | LOC105377419 - LOC105377420; LOC105377419 - LOC105377420; LOC105377419 - LOC105377420; LOC105377419 - LOC105377420 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11099040-?; rs13113376-?; rs1908039-?; rs1908038-? |
SNPs | rs11099040; rs13113376; rs1908039; rs1908038 |
Merged | 0 |
SNP id current | |
Context | intergenic_variant; intergenic_variant; intergenic_variant; intergenic_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.00000009 |
Pvalue mlog | 7.04575749056067 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Illumina [795637] |
CNV | N |
Mapped trait | intelligence |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004337 |
Study accession | GCST001428 |