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.