rs181489
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs181489(C;C) |
| Make rs181489(C;T) |
| Make rs181489(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 89713869 |
| Gene | LOC105377329 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs181489 |
| dbSNP (classic) | rs181489 |
| ClinGen | rs181489 |
| ebi | rs181489 |
| HLI | rs181489 |
| Exac | rs181489 |
| Gnomad | rs181489 |
| Varsome | rs181489 |
| LitVar | rs181489 |
| Map | rs181489 |
| PheGenI | rs181489 |
| Biobank | rs181489 |
| 1000 genomes | rs181489 |
| hgdp | rs181489 |
| ensembl | rs181489 |
| geneview | rs181489 |
| scholar | rs181489 |
| rs181489 | |
| pharmgkb | rs181489 |
| gwascentral | rs181489 |
| openSNP | rs181489 |
| 23andMe | rs181489 |
| SNPshot | rs181489 |
| SNPdbe | rs181489 |
| MSV3d | rs181489 |
| GWAS Ctlg | rs181489 |
| GMAF | 0.1979 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23962496
] The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
[PMID 21391235] Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.
[PMID 25656566] Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta-analysis
[PMID 30410434] A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.
