rs1011313
| Orientation | minus |
| Stabilized | minus |
| Make rs1011313(A;A) |
| Make rs1011313(A;G) |
| Make rs1011313(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 15633201 |
| Gene | DTNBP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1011313 |
| dbSNP (classic) | rs1011313 |
| ClinGen | rs1011313 |
| ebi | rs1011313 |
| HLI | rs1011313 |
| Exac | rs1011313 |
| Gnomad | rs1011313 |
| Varsome | rs1011313 |
| LitVar | rs1011313 |
| Map | rs1011313 |
| PheGenI | rs1011313 |
| Biobank | rs1011313 |
| 1000 genomes | rs1011313 |
| hgdp | rs1011313 |
| ensembl | rs1011313 |
| geneview | rs1011313 |
| scholar | rs1011313 |
| rs1011313 | |
| pharmgkb | rs1011313 |
| gwascentral | rs1011313 |
| openSNP | rs1011313 |
| 23andMe | rs1011313 |
| SNPshot | rs1011313 |
| SNPdbe | rs1011313 |
| MSV3d | rs1011313 |
| GWAS Ctlg | rs1011313 |
| GMAF | 0.1171 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 19077176] Variation in the dysbindin gene and normal cognitive function in three independent population samples
[PMID 19252939] Dysbindin gene (DTNBP1) and schizophrenia in Korean population
[PMID 19937977] Association study of NRG1, DTNBP1, RGS4, G72/G30, and PIP5K2A with schizophrenia and symptom severity in a Hungarian sample
[PMID 12098102
] Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia.
[PMID 12474144] Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families.
[PMID 14618545] The DTNBP1 (dysbindin) gene contributes to schizophrenia, depending on family history of the disease.
[PMID 15290652] A powerful strategy to account for multiple testing in the context of haplotype analysis.
[PMID 15362017] Association of the DTNBP1 locus with schizophrenia in a U.S. population.
[PMID 17033966] Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia.
[PMID 17074466] DTNBP1 genotype influences cognitive decline in schizophrenia.
[PMID 17192893] Effect of 5-haplotype of dysbindin gene (DTNBP1) polymorphisms for the susceptibility to bipolar I disorder.
[PMID 17264804] Dysbindin associated with selective serotonin reuptake inhibitor antidepressant efficacy.
[PMID 17445278] Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblings.
[PMID 17888175] Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia.
[PMID 17964051] Is there protective haplotype of dysbindin gene (DTNBP1) 3 polymorphisms for major depressive disorder.
[PMID 18562100] DTNBP1 haplotype influences baseline assessment scores of schizophrenic in-patients.
[PMID 18663367] The dystrobrevin-binding protein 1 gene: features and networks.
[PMID 18715757] Genetic associations with schizophrenia: meta-analyses of 12 candidate genes.
[PMID 18797396] Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depression.
[PMID 18804346] Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia.
[PMID 19089808] Association of the dystrobrevin binding protein 1 gene (DTNBP1) in a bipolar case-control study (BACCS).
[PMID 19911060] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.
[PMID 20046352] Effect of the dysbindin gene on antimanic agents in patients with bipolar I disorder.
