Human SNP ID | rs16973500 |
---|---|
Human chromosome | chr16 |
Human SNP position | 71931293 |
Pig chromosome | JH118898-1 |
Pig SNP position | 145164 |
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 | 16q22.2 |
Chromosome id | chr16 |
Chromosome position | 71931293 |
Reported gene | PKD1L3, KIAA0174, DHODH |
Mapped gene | PKD1L3 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 342372 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs16973500-C |
SNPs | rs16973500 |
Merged | 0 |
SNP id current | 16973500 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.86 |
P value | 0.000007 |
Pvalue mlog | 5.15490195998574 |
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 |