Human SNP ID | rs34312136 |
---|---|
Human chromosome | chr9 |
Human SNP position | 134377610 |
Pig chromosome | chr1 |
Pig SNP position | 307721792 |
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 | 9q34.2 |
Chromosome id | chr9;9;9;9 |
Chromosome position | 134389093;134393077;134393657;134377610 |
Reported gene | RXRA |
Mapped gene | RXRA; RXRA; RXRA; RXRA |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs35079168-?; rs4501664-?; rs11102986-?; rs34312136-? |
SNPs | rs35079168; rs4501664; rs11102986; rs34312136 |
Merged | 0 |
SNP id current | |
Context | intron_variant; intron_variant; intron_variant; intron_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.00000008 |
Pvalue mlog | 7.09691001300805 |
P value text | (Schizophrenia, Cognitive ability) |
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 |