Human SNP ID | rs10831284 |
---|---|
Human chromosome | chr11 |
Human SNP position | 94934799 |
Pig chromosome | chr9 |
Pig SNP position | 30767465 |
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 | 11q21 |
Chromosome id | chr11 |
Chromosome position | 94934799 |
Reported gene | AMOTL1, CWC15, JMJD2D |
Mapped gene | AMOTL1 - CWC15 |
Upstream gene id | 154810 |
Downstream gene id | 51503 |
SNP gene ids | |
Upstream gene distance | 58046 |
Downstream gene distance | 27823 |
SNP risk allele | rs10831284-G |
SNPs | rs10831284 |
Merged | 0 |
SNP id current | 10831284 |
Context | regulatory_region_variant |
Intergenic | 1 |
Allele frequency | 0.13 |
P value | 0.000002 |
Pvalue mlog | 5.69897000433601 |
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 |