Human SNP ID | rs11838918 |
---|---|
Human chromosome | chr13 |
Human SNP position | 78836439 |
Pig chromosome | chr11 |
Pig SNP position | 55703720 |
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 | 13q31.1 |
Chromosome id | chr13 |
Chromosome position | 78836439 |
Reported gene | intergenic |
Mapped gene | LINC00331 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100874126 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11838918-C |
SNPs | rs11838918 |
Merged | 0 |
SNP id current | 11838918 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.022 |
P value | 0.00000001 |
Pvalue mlog | 8 |
P value text | |
Or beta | 0.28 |
%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 |
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 | 13q31.1 |
Chromosome id | chr13 |
Chromosome position | 78836439 |
Reported gene | intergenic |
Mapped gene | LINC00331 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100874126 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11838918-C |
SNPs | rs11838918 |
Merged | 0 |
SNP id current | 11838918 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.022 |
P value | 0.000003 |
Pvalue mlog | 5.52287874528033 |
P value text | |
Or beta | 2.26 |
%95 Ci | [1.61-3.18] |
Platform | Illumina [948658] |
CNV | N |
Mapped trait | conduct disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0004216 |
Study accession | GCST000714 |
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 | 13q31.1 |
Chromosome id | chr13 |
Chromosome position | 78836439 |
Reported gene | intergenic |
Mapped gene | LINC00331 |
Upstream gene id | |
Downstream gene id | |
SNP gene ids | 100874126 |
Upstream gene distance | |
Downstream gene distance | |
SNP risk allele | rs11838918-C |
SNPs | rs11838918 |
Merged | 0 |
SNP id current | 11838918 |
Context | intergenic_variant |
Intergenic | 0 |
Allele frequency | 0.066 |
P value | 0.0000003 |
Pvalue mlog | 6.52287874528033 |
P value text | (AA) |
Or beta | 0.278 |
%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 |