rs148322402
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs148322402(A;A) |
| Make rs148322402(A;G) |
| Make rs148322402(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 7 |
| Position | 102070411 |
| Gene | CUX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs148322402 |
| dbSNP (classic) | rs148322402 |
| ClinGen | rs148322402 |
| ebi | rs148322402 |
| HLI | rs148322402 |
| Exac | rs148322402 |
| Gnomad | rs148322402 |
| Varsome | rs148322402 |
| LitVar | rs148322402 |
| Map | rs148322402 |
| PheGenI | rs148322402 |
| Biobank | rs148322402 |
| 1000 genomes | rs148322402 |
| hgdp | rs148322402 |
| ensembl | rs148322402 |
| geneview | rs148322402 |
| scholar | rs148322402 |
| rs148322402 | |
| pharmgkb | rs148322402 |
| gwascentral | rs148322402 |
| openSNP | rs148322402 |
| 23andMe | rs148322402 |
| SNPshot | rs148322402 |
| SNPdbe | rs148322402 |
| MSV3d | rs148322402 |
| GWAS Ctlg | rs148322402 |
| 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.
