rs1521882
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs1521882(C;C) |
| Make rs1521882(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 202085128 |
| Gene | KIAA2012 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1521882 |
| dbSNP (classic) | rs1521882 |
| ClinGen | rs1521882 |
| ebi | rs1521882 |
| HLI | rs1521882 |
| Exac | rs1521882 |
| Gnomad | rs1521882 |
| Varsome | rs1521882 |
| LitVar | rs1521882 |
| Map | rs1521882 |
| PheGenI | rs1521882 |
| Biobank | rs1521882 |
| 1000 genomes | rs1521882 |
| hgdp | rs1521882 |
| ensembl | rs1521882 |
| geneview | rs1521882 |
| scholar | rs1521882 |
| rs1521882 | |
| pharmgkb | rs1521882 |
| gwascentral | rs1521882 |
| openSNP | rs1521882 |
| 23andMe | rs1521882 |
| SNPshot | rs1521882 |
| SNPdbe | rs1521882 |
| MSV3d | rs1521882 |
| GWAS Ctlg | rs1521882 |
| GMAF | 0.2025 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18951430] |
| Trait | Attention-deficit/hyperactivity disorder and conduct disorder |
| Title | Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
| Risk Allele | A |
| P-val | 0.000008 |
| Odds Ratio | NR NR |
