rs9370822
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9370822(A;A) |
| Make rs9370822(A;C) |
| Make rs9370822(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 15544505 |
| Gene | DTNBP1, LOC105374947 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9370822 |
| dbSNP (classic) | rs9370822 |
| ClinGen | rs9370822 |
| ebi | rs9370822 |
| HLI | rs9370822 |
| Exac | rs9370822 |
| Gnomad | rs9370822 |
| Varsome | rs9370822 |
| LitVar | rs9370822 |
| Map | rs9370822 |
| PheGenI | rs9370822 |
| Biobank | rs9370822 |
| 1000 genomes | rs9370822 |
| hgdp | rs9370822 |
| ensembl | rs9370822 |
| geneview | rs9370822 |
| scholar | rs9370822 |
| rs9370822 | |
| pharmgkb | rs9370822 |
| gwascentral | rs9370822 |
| openSNP | rs9370822 |
| 23andMe | rs9370822 |
| SNPshot | rs9370822 |
| SNPdbe | rs9370822 |
| MSV3d | rs9370822 |
| GWAS Ctlg | rs9370822 |
| GMAF | 0.444 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
[PMID 20615671] Analysis of HapMap tag-SNPs in dysbindin (DTNBP1) reveals evidence of consistent association with schizophrenia
[PMID 20615259
] A polymorphism in the dysbindin gene (DTNBP1) associated with multiple psychiatric disorders including schizophrenia
[PMID 17033966] Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia.
[PMID 20951386] Dysbindin (DTNBP1)--a role in psychotic depression?
