rs4792394
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4792394(A;A) |
| Make rs4792394(A;C) |
| Make rs4792394(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 13781600 |
| Gene | LOC107985014 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4792394 |
| dbSNP (classic) | rs4792394 |
| ClinGen | rs4792394 |
| ebi | rs4792394 |
| HLI | rs4792394 |
| Exac | rs4792394 |
| Gnomad | rs4792394 |
| Varsome | rs4792394 |
| LitVar | rs4792394 |
| Map | rs4792394 |
| PheGenI | rs4792394 |
| Biobank | rs4792394 |
| 1000 genomes | rs4792394 |
| hgdp | rs4792394 |
| ensembl | rs4792394 |
| geneview | rs4792394 |
| scholar | rs4792394 |
| rs4792394 | |
| pharmgkb | rs4792394 |
| gwascentral | rs4792394 |
| openSNP | rs4792394 |
| 23andMe | rs4792394 |
| SNPshot | rs4792394 |
| SNPdbe | rs4792394 |
| MSV3d | rs4792394 |
| GWAS Ctlg | rs4792394 |
| GMAF | 0.4288 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (symptom count) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 0.000009 |
| Odds Ratio | 0.06 [NR] unit decrease |
