rs10492664
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs10492664(A;A) |
| Make rs10492664(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 108163877 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10492664 |
| dbSNP (classic) | rs10492664 |
| ClinGen | rs10492664 |
| ebi | rs10492664 |
| HLI | rs10492664 |
| Exac | rs10492664 |
| Gnomad | rs10492664 |
| Varsome | rs10492664 |
| LitVar | rs10492664 |
| Map | rs10492664 |
| PheGenI | rs10492664 |
| Biobank | rs10492664 |
| 1000 genomes | rs10492664 |
| hgdp | rs10492664 |
| ensembl | rs10492664 |
| geneview | rs10492664 |
| scholar | rs10492664 |
| rs10492664 | |
| pharmgkb | rs10492664 |
| gwascentral | rs10492664 |
| openSNP | rs10492664 |
| 23andMe | rs10492664 |
| SNPshot | rs10492664 |
| SNPdbe | rs10492664 |
| MSV3d | rs10492664 |
| GWAS Ctlg | rs10492664 |
| GMAF | 0.2236 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 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 | C |
| P-val | 0.000001 |
| Odds Ratio | NR NR |
