rs356182
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) |
| Make rs356182(C;T) |
| Make rs356182(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 4 |
| Position | 89704960 |
| Gene | LOC105377329 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs356182 |
| dbSNP (classic) | rs356182 |
| ClinGen | rs356182 |
| ebi | rs356182 |
| HLI | rs356182 |
| Exac | rs356182 |
| Gnomad | rs356182 |
| Varsome | rs356182 |
| LitVar | rs356182 |
| Map | rs356182 |
| PheGenI | rs356182 |
| Biobank | rs356182 |
| 1000 genomes | rs356182 |
| hgdp | rs356182 |
| ensembl | rs356182 |
| geneview | rs356182 |
| scholar | rs356182 |
| rs356182 | |
| pharmgkb | rs356182 |
| gwascentral | rs356182 |
| openSNP | rs356182 |
| 23andMe | rs356182 |
| SNPshot | rs356182 |
| SNPdbe | rs356182 |
| MSV3d | rs356182 |
| GWAS Ctlg | rs356182 |
| Max Magnitude | 0 |
http://medicalxpress.com/news/2016-04-uncovers-genetic-variation-physical-decline.html parkinson's disease
[PMID 27538639] SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.
