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rs387907571(A;G)

From SNPedia

Parkinson's disease, possible
Is agenotype
ofrs387907571
GeneDNAJC13
Chromosome3
Position132,477,995
mentionedby
Magnitude6
ReputeBad
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.