rs7762160
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7762160(C;C) |
| Make rs7762160(C;T) |
| Make rs7762160(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 165601943 |
| Gene | PDE10A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7762160 |
| dbSNP (classic) | rs7762160 |
| ClinGen | rs7762160 |
| ebi | rs7762160 |
| HLI | rs7762160 |
| Exac | rs7762160 |
| Gnomad | rs7762160 |
| Varsome | rs7762160 |
| LitVar | rs7762160 |
| Map | rs7762160 |
| PheGenI | rs7762160 |
| Biobank | rs7762160 |
| 1000 genomes | rs7762160 |
| hgdp | rs7762160 |
| ensembl | rs7762160 |
| geneview | rs7762160 |
| scholar | rs7762160 |
| rs7762160 | |
| pharmgkb | rs7762160 |
| gwascentral | rs7762160 |
| openSNP | rs7762160 |
| 23andMe | rs7762160 |
| SNPshot | rs7762160 |
| SNPdbe | rs7762160 |
| MSV3d | rs7762160 |
| GWAS Ctlg | rs7762160 |
| GMAF | 0.3462 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (symptom count) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | 0.07 [NR] unit increase |
