Human SNP ID | rs7589014 |
---|---|
Human chromosome | chr2 |
Human SNP position | 200716231 |
Pig chromosome | chr15 |
Pig SNP position | 115539595 |
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 | 2q33.1 |
Chromosome id | chr2;2;2;2 |
Chromosome position | 200706420;200716231;200717470;200711561 |
Reported gene | AOX1 |
Mapped gene | AOX2P; AOX2P; LOC100507140; AOX2P; LOC100507140; AOX2P |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs2540051-?; rs7589014-?; rs2348114-?; rs7563911-? |
SNPs | rs2540051; rs7589014; rs2348114; rs7563911 |
Merged | 0 |
SNP id current | |
Context | splice_donor_variant; intron_variant; non_coding_transcript_exon_variant; intron_variant |
Intergenic | |
Allele frequency | NR |
P value | 0.00000006 |
Pvalue mlog | 7.22184874961635 |
P value text | (Amyotrophic Lateral Sclerosis) |
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 |