rs1391768
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1391768(C;C) |
| Make rs1391768(C;T) |
| Make rs1391768(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 8437548 |
| Gene | NDEL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1391768 |
| dbSNP (classic) | rs1391768 |
| ClinGen | rs1391768 |
| ebi | rs1391768 |
| HLI | rs1391768 |
| Exac | rs1391768 |
| Gnomad | rs1391768 |
| Varsome | rs1391768 |
| LitVar | rs1391768 |
| Map | rs1391768 |
| PheGenI | rs1391768 |
| Biobank | rs1391768 |
| 1000 genomes | rs1391768 |
| hgdp | rs1391768 |
| ensembl | rs1391768 |
| geneview | rs1391768 |
| scholar | rs1391768 |
| rs1391768 | |
| pharmgkb | rs1391768 |
| gwascentral | rs1391768 |
| openSNP | rs1391768 |
| 23andMe | rs1391768 |
| SNPshot | rs1391768 |
| SNPdbe | rs1391768 |
| MSV3d | rs1391768 |
| GWAS Ctlg | rs1391768 |
| GMAF | 0.4109 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18469341
] 275 Caucasian schizophrenia patients and 200 controls rs1391768 imparting a significant effect but only in the context of a Cys carrying background
[PMID 19251251] Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.
