rs143573515
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs143573515(C;C) |
| Make rs143573515(C;T) |
| Make rs143573515(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 3 |
| Position | 49531818 |
| Gene | DAG1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs143573515 |
| dbSNP (classic) | rs143573515 |
| ClinGen | rs143573515 |
| ebi | rs143573515 |
| HLI | rs143573515 |
| Exac | rs143573515 |
| Gnomad | rs143573515 |
| Varsome | rs143573515 |
| LitVar | rs143573515 |
| Map | rs143573515 |
| PheGenI | rs143573515 |
| Biobank | rs143573515 |
| 1000 genomes | rs143573515 |
| hgdp | rs143573515 |
| ensembl | rs143573515 |
| geneview | rs143573515 |
| scholar | rs143573515 |
| rs143573515 | |
| pharmgkb | rs143573515 |
| gwascentral | rs143573515 |
| openSNP | rs143573515 |
| 23andMe | rs143573515 |
| SNPshot | rs143573515 |
| SNPdbe | rs143573515 |
| MSV3d | rs143573515 |
| GWAS Ctlg | rs143573515 |
| 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.
| ClinVar | |
|---|---|
| Risk | rs143573515(T;T) |
| Alt | rs143573515(T;T) |
| Reference | rs143573515(C;C) |
| Significance | Unknown |
| Disease | not specified |
| Variation | info |
| Gene | DAG1 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000003.11:g.49569251C>T |
| CLNSRC | |
| CLNACC | RCV000373932.1, |
