rs760678
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs760678(C;C) |
| Make rs760678(C;G) |
| Make rs760678(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 11334421 |
| Gene | LOC105374925, NEDD9 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs760678 |
| dbSNP (classic) | rs760678 |
| ClinGen | rs760678 |
| ebi | rs760678 |
| HLI | rs760678 |
| Exac | rs760678 |
| Gnomad | rs760678 |
| Varsome | rs760678 |
| LitVar | rs760678 |
| Map | rs760678 |
| PheGenI | rs760678 |
| Biobank | rs760678 |
| 1000 genomes | rs760678 |
| hgdp | rs760678 |
| ensembl | rs760678 |
| geneview | rs760678 |
| scholar | rs760678 |
| rs760678 | |
| pharmgkb | rs760678 |
| gwascentral | rs760678 |
| openSNP | rs760678 |
| 23andMe | rs760678 |
| SNPshot | rs760678 |
| SNPdbe | rs760678 |
| MSV3d | rs760678 |
| GWAS Ctlg | rs760678 |
| GMAF | 0.2984 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20430066] DIFFERENT IMPLICATION OF NEDD9 GENETIC VARIANT IN EARLY AND LATE ONSET ALZHEIMER'S DISEASE
[PMID 21059344] NEDD9 is genetically associated with Alzheimer's disease in a Han Chinese population
[PMID 18579580] Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease.
[PMID 21399483] NEDD9 gene polymorphism influences the risk of Alzheimer disease and cognitive function in Chinese older persons.
[PMID 22963925] NEDD9 rs760678 polymorphism and the risk of Alzheimer's disease: A meta-analysis
