Human SNP ID | rs2184898 |
---|---|
Human chromosome | chr10 |
Human SNP position | 117658593 |
Pig chromosome | chr14 |
Pig SNP position | 139152386 |
PubMed ID | 20585324 |
---|---|
Journal | Mol Psychiatry |
Link | www.ncbi.nlm.nih.gov/pubmed/20585324 |
Study | Genome-wide association study of conduct disorder symptomatology. |
Disease/Trait | Conduct disorder |
Initial sample | 872 European, African American and other ancestry substance dependence cases, 3,091 European, African American and other ancestry controls |
Replication sample | NA |
Region | 10q26.11 |
Chromosome id | chr10 |
Chromosome position | 117658593 |
Reported gene | intergenic |
Mapped gene | EMX2 - LOC102724627 |
Upstream gene id | 2018 |
Downstream gene id | 102724627 |
SNP gene ids | |
Upstream gene distance | 109047 |
Downstream gene distance | 76341 |
SNP risk allele | rs2184898-A |
SNPs | rs2184898 |
Merged | 0 |
SNP id current | 2184898 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | 0.327 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 1.33 |
%95 Ci | [1.18-1.50] |
Platform | Illumina [948658] |
CNV | N |
Mapped trait | conduct disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004216 |
Study accession | GCST000714 |