rs1550057
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1550057(C;C) |
| Make rs1550057(C;T) |
| Make rs1550057(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 141196270 |
| Gene | RNF150 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1550057 |
| dbSNP (classic) | rs1550057 |
| ClinGen | rs1550057 |
| ebi | rs1550057 |
| HLI | rs1550057 |
| Exac | rs1550057 |
| Gnomad | rs1550057 |
| Varsome | rs1550057 |
| LitVar | rs1550057 |
| Map | rs1550057 |
| PheGenI | rs1550057 |
| Biobank | rs1550057 |
| 1000 genomes | rs1550057 |
| hgdp | rs1550057 |
| ensembl | rs1550057 |
| geneview | rs1550057 |
| scholar | rs1550057 |
| rs1550057 | |
| pharmgkb | rs1550057 |
| gwascentral | rs1550057 |
| openSNP | rs1550057 |
| 23andMe | rs1550057 |
| SNPshot | rs1550057 |
| SNPdbe | rs1550057 |
| MSV3d | rs1550057 |
| GWAS Ctlg | rs1550057 |
| GMAF | 0.3347 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (case status) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 0.000004 |
| Odds Ratio | 1.39 [1.21-1.61] |
