rs387907571(A;G)
From SNPedia
| Parkinson's disease, possible |
| Is a | genotype |
| of | rs387907571 |
| Gene | DNAJC13 |
| Chromosome | 3 |
| Position | 132,477,995 |
| mentioned | by |
| Magnitude | 6 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 6 | Parkinson's disease, possible |
The rare (G) allele for this mutation is reported to be an autosomal dominant mutation causing Parkinson's disease. See discussion at rs387907571.
