Human SNP ID | rs1644305 |
---|---|
Human chromosome | chr5 |
Human SNP position | 133867905 |
Pig chromosome | chr2 |
Pig SNP position | 141753452 |
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 | 5q31.1 |
Chromosome id | chr5 |
Chromosome position | 133867905 |
Reported gene | C5orf15 |
Mapped gene | FSTL4 - LOC105379182 |
Upstream gene id | 23105 |
Downstream gene id | 105379182 |
SNP gene ids | |
Upstream gene distance | 25839 |
Downstream gene distance | 59829 |
SNP risk allele | rs1644305-A |
SNPs | rs1644305 |
Merged | 0 |
SNP id current | 1644305 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.41 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
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 |