Rs10492664
From SNPedia
| Orientation | minus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10492664 |
| PheGenI | rs10492664 |
| nextbio | rs10492664 |
| hapmap | rs10492664 |
| 1000 genomes | rs10492664 |
| hgdp | rs10492664 |
| ensembl | rs10492664 |
| gopubmed | rs10492664 |
| geneview | rs10492664 |
| scholar | rs10492664 |
| rs10492664 | |
| pharmgkb | rs10492664 |
| gwascentral | rs10492664 |
| openSNP | rs10492664 |
| 23andMe | rs10492664 |
| 23andMe all | rs10492664 |
| SNP Nexus | |
| SNPshot | rs10492664 |
| SNPdbe | rs10492664 |
| MSV3d | rs10492664 |
| Chromosome | 13 |
| Orientation | minus |
| GMAF | 0.223 |
| Position | 108816225 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in complete genomics |
| Make rs10492664(A;A) |
| Make rs10492664(A;G) |
| ? | (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 |
| GET Evidence | |
|---|---|
| rs10492664 | |
| aa_change | |
| aa_change_short | |
| impact | pathogenic |
| qualified_impact | Insufficiently evaluated pathogenic |
| overall_frequency | 0.25 |
| summary | |
