rs111596332
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs111596332(A;A) |
| Make rs111596332(A;G) |
| Make rs111596332(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 20 |
| Position | 31476659 |
| Gene | DEFB124, REM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs111596332 |
| dbSNP (classic) | rs111596332 |
| ClinGen | rs111596332 |
| ebi | rs111596332 |
| HLI | rs111596332 |
| Exac | rs111596332 |
| Gnomad | rs111596332 |
| Varsome | rs111596332 |
| LitVar | rs111596332 |
| Map | rs111596332 |
| PheGenI | rs111596332 |
| Biobank | rs111596332 |
| 1000 genomes | rs111596332 |
| hgdp | rs111596332 |
| ensembl | rs111596332 |
| geneview | rs111596332 |
| scholar | rs111596332 |
| rs111596332 | |
| pharmgkb | rs111596332 |
| gwascentral | rs111596332 |
| openSNP | rs111596332 |
| 23andMe | rs111596332 |
| SNPshot | rs111596332 |
| SNPdbe | rs111596332 |
| MSV3d | rs111596332 |
| GWAS Ctlg | rs111596332 |
| Max Magnitude | 0 |
[PMID 27120077
] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.
