rs3136202
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3136202(A;A) |
| Make rs3136202(A;G) |
| Make rs3136202(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 13944317 |
| Gene | ERCC4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3136202 |
| dbSNP (classic) | rs3136202 |
| ClinGen | rs3136202 |
| ebi | rs3136202 |
| HLI | rs3136202 |
| Exac | rs3136202 |
| Gnomad | rs3136202 |
| Varsome | rs3136202 |
| LitVar | rs3136202 |
| Map | rs3136202 |
| PheGenI | rs3136202 |
| Biobank | rs3136202 |
| 1000 genomes | rs3136202 |
| hgdp | rs3136202 |
| ensembl | rs3136202 |
| geneview | rs3136202 |
| scholar | rs3136202 |
| rs3136202 | |
| pharmgkb | rs3136202 |
| gwascentral | rs3136202 |
| openSNP | rs3136202 |
| 23andMe | rs3136202 |
| SNPshot | rs3136202 |
| SNPdbe | rs3136202 |
| MSV3d | rs3136202 |
| GWAS Ctlg | rs3136202 |
| GMAF | 0.3756 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (symptom count) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | 0.07 [NR] unit decrease |
