rs356229
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs356229(A;A) |
| Make rs356229(A;G) |
| Make rs356229(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 89685446 |
| Gene | LOC105377329 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs356229 |
| dbSNP (classic) | rs356229 |
| ClinGen | rs356229 |
| ebi | rs356229 |
| HLI | rs356229 |
| Exac | rs356229 |
| Gnomad | rs356229 |
| Varsome | rs356229 |
| LitVar | rs356229 |
| Map | rs356229 |
| PheGenI | rs356229 |
| Biobank | rs356229 |
| 1000 genomes | rs356229 |
| hgdp | rs356229 |
| ensembl | rs356229 |
| geneview | rs356229 |
| scholar | rs356229 |
| rs356229 | |
| pharmgkb | rs356229 |
| gwascentral | rs356229 |
| openSNP | rs356229 |
| 23andMe | rs356229 |
| SNPshot | rs356229 |
| SNPdbe | rs356229 |
| MSV3d | rs356229 |
| GWAS Ctlg | rs356229 |
| GMAF | 0.259 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21058943
] Replication of GWAS associations for GAK and MAPT in Parkinson's disease
[PMID 15637659] Linkage disequilibrium patterns and tagSNP transferability among European populations.
[PMID 18985386] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
[PMID 19771175] Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
[PMID 22425546] SNCA polymorphisms, smoking, and sporadic Parkinson's disease in Japanese.
