rs387907571(A;G)

Parkinson's disease, possible

Magnitude
6.0Very important
Repute
Bad
On SNPedia
rs387907571(A;G)
Gene
DNAJC13

Other genotypes of rs387907571

  1. A;AGoodcommon in clinvarTypical · 0.0

All about rs387907571

Notes

From SNPedia

The rare (G) allele for this mutation is reported to be an autosomal dominant mutation causing Parkinson's disease. See discussion at rs387907571.

Source and license

Adapted from rs387907571(A;G) on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.