Human SNP ID | rs4533251 |
---|---|
Human chromosome | chr15 |
Human SNP position | 96719197 |
Pig chromosome | chr7 |
Pig SNP position | 88670311 |
PubMed ID | 18951430 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18951430 |
Study | Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. |
Disease/Trait | Attention deficit hyperactivity disorder and conduct disorder |
Initial sample | 938 European ancestry trios |
Replication sample | NA |
Region | 15q26.2 |
Chromosome id | chr15 |
Chromosome position | 96719197 |
Reported gene | SPATA8 |
Mapped gene | LOC105371002 - SPATA8-AS1 |
Upstream gene id | 105371002 |
Downstream gene id | 100652749 |
SNP gene ids | |
Upstream gene distance | 14331 |
Downstream gene distance | 52808 |
SNP risk allele | rs4533251-T |
SNPs | rs4533251 |
Merged | 0 |
SNP id current | 4533251 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.15 |
P value | 0.000004 |
Pvalue mlog | 5.39794000867203 |
P value text | |
Or beta | |
%95 Ci | |
Platform | Perlegen [378332] |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder, conduct disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004216 |
Study accession | GCST000253 |