Human SNP ID | rs12302829 |
---|---|
Human chromosome | chr12 |
Human SNP position | 5031318 |
Pig chromosome | chr5 |
Pig SNP position | 67668773 |
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 (symptom count) |
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 | 12p13.32 |
Chromosome id | chr12 |
Chromosome position | 5031318 |
Reported gene | intergenic |
Mapped gene | LOC100507560 - LOC390282 |
Upstream gene id | 100507560 |
Downstream gene id | 390282 |
SNP gene ids | |
Upstream gene distance | 5724 |
Downstream gene distance | 1073 |
SNP risk allele | rs12302829-G |
SNPs | rs12302829 |
Merged | 0 |
SNP id current | 12302829 |
Context | downstream_gene_variant |
Intergenic | 1 |
Allele frequency | 0.008 |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | |
Or beta | 0.35 |
%95 Ci | [NR] unit decrease |
Platform | Illumina [948658] |
CNV | N |
Mapped trait | conduct disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004216 |
Study accession | GCST000713 |