rs10513789
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 1.8 | 0.64x decreased risk of Parkinson's disease |
| (G;T) | 1.4 | 0.8x decreased risk of Parkinson's disease |
| (T;T) | 1.25 | Very common. Normal risk of Parkinson's disease. |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 183042285 |
| Gene | MCCC1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10513789 |
| dbSNP (classic) | rs10513789 |
| ClinGen | rs10513789 |
| ebi | rs10513789 |
| HLI | rs10513789 |
| Exac | rs10513789 |
| Gnomad | rs10513789 |
| Varsome | rs10513789 |
| LitVar | rs10513789 |
| Map | rs10513789 |
| PheGenI | rs10513789 |
| Biobank | rs10513789 |
| 1000 genomes | rs10513789 |
| hgdp | rs10513789 |
| ensembl | rs10513789 |
| geneview | rs10513789 |
| scholar | rs10513789 |
| rs10513789 | |
| pharmgkb | rs10513789 |
| gwascentral | rs10513789 |
| openSNP | rs10513789 |
| 23andMe | rs10513789 |
| SNPshot | rs10513789 |
| SNPdbe | rs10513789 |
| MSV3d | rs10513789 |
| GWAS Ctlg | rs10513789 |
| GMAF | 0.3264 |
| Max Magnitude | 1.8 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
23andMe reports that the G allele of rs10513789 is associated with 0.8 times lower odds of Parkinson's disease. [PMID 21738487
]
23andMe has a patent covering this snp. http://blog.23andme.com/2012/05/28/announcing-23andmes-first-patent/
