Human SNP ID | rs7236632 |
---|---|
Human chromosome | chr18 |
Human SNP position | 57766970 |
Pig chromosome | chr1 |
Pig SNP position | 180583568 |
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 | 18q21.31 |
Chromosome id | chr18 |
Chromosome position | 57766970 |
Reported gene | ATP8B1 |
Mapped gene | LOC105376870, ATP8B1 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105376870, 5205 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs7236632-A |
SNPs | rs7236632 |
Merged | 0 |
SNP id current | 7236632 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.86 |
P value | 0.000006 |
Pvalue mlog | 5.22184874961635 |
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 |