rs13398848
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs13398848(A;G) |
| Make rs13398848(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 84018044 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13398848 |
| dbSNP (classic) | rs13398848 |
| ClinGen | rs13398848 |
| ebi | rs13398848 |
| HLI | rs13398848 |
| Exac | rs13398848 |
| Gnomad | rs13398848 |
| Varsome | rs13398848 |
| LitVar | rs13398848 |
| Map | rs13398848 |
| PheGenI | rs13398848 |
| Biobank | rs13398848 |
| 1000 genomes | rs13398848 |
| hgdp | rs13398848 |
| ensembl | rs13398848 |
| geneview | rs13398848 |
| scholar | rs13398848 |
| rs13398848 | |
| pharmgkb | rs13398848 |
| gwascentral | rs13398848 |
| openSNP | rs13398848 |
| 23andMe | rs13398848 |
| SNPshot | rs13398848 |
| SNPdbe | rs13398848 |
| MSV3d | rs13398848 |
| GWAS Ctlg | rs13398848 |
| GMAF | 0.08219 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (case status) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | 1.59 [1.30-1.95] |
