Human SNP ID | rs8179116 |
---|---|
Human chromosome | chr12 |
Human SNP position | 108631651 |
Pig chromosome | chr14 |
Pig SNP position | 44712176 |
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 | 12q24.11 |
Chromosome id | chr12 |
Chromosome position | 108631651 |
Reported gene | SELPLG |
Mapped gene | LOC105369968, SELPLG |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 105369968, 6404 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs8179116-A |
SNPs | rs8179116 |
Merged | 0 |
SNP id current | 8179116 |
Context | intron_variant |
Intergenic | 0 |
Allele frequency | 0.021 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 0.23 |
%95 Ci | [NR] unit increase |
Platform | Illumina [948658] |
CNV | N |
Mapped trait | conduct disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004216 |
Study accession | GCST000713 |