rs9370399
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9370399(A;A) |
| Make rs9370399(A;C) |
| Make rs9370399(C;C) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 6 |
| Position | 55180227 |
| Gene | HCRTR2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9370399 |
| dbSNP (classic) | rs9370399 |
| ClinGen | rs9370399 |
| ebi | rs9370399 |
| HLI | rs9370399 |
| Exac | rs9370399 |
| Gnomad | rs9370399 |
| Varsome | rs9370399 |
| LitVar | rs9370399 |
| Map | rs9370399 |
| PheGenI | rs9370399 |
| Biobank | rs9370399 |
| 1000 genomes | rs9370399 |
| hgdp | rs9370399 |
| ensembl | rs9370399 |
| geneview | rs9370399 |
| scholar | rs9370399 |
| rs9370399 | |
| pharmgkb | rs9370399 |
| gwascentral | rs9370399 |
| openSNP | rs9370399 |
| 23andMe | rs9370399 |
| SNPshot | rs9370399 |
| SNPdbe | rs9370399 |
| MSV3d | rs9370399 |
| GWAS Ctlg | rs9370399 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 27335043] Lack of association between genetic polymorphism of circadian genes (PER2, PER3, CLOCK and OX2R) with late onset depression and Alzheimer's disease in a sample of a Brazilian population (Circadian Genes, Late-Onset Depression and Alzheimer's Disease).
