Parkinson’s disease

Improve outcomes through precision results

For patients with a family history of Parkinson’s disease, understanding their genetic risk of developing the condition is an important first step in tailoring interventions that may delay symptom onset and progression.

Genetic testing can reveal characteristics about prognosis and may help guide and customize treatment selection. Genetic testing is also important for patients affected by early-onset illness, which is more often due to genetic causes. Although known genetic variation is present in only 10% to 15% of patients, awareness regarding specific genetic causes can deepen understanding about disease progression and enable elevated outcomes.

Parkinson’s disease Test menu

Parkinson’s disease

Our comprehensive Parkinson’s disease gene panel was developed by a multidisciplinary team of clinicians, geneticists, and laboratory testing experts, and includes genes known for causing Parkinson’s disease, but also genes that increase the likelihood of developing the condition.

Key testing


  • Uses next-generation sequencing to detect single nucleotides and copy number variants in 94 genes associated with Parkinson’s disease.
  • Establishes molecular diagnosis.
  • Identifies variants within genes known to be associated with Parkinson’s disease, enabling predictive testing for at-risk family members.
  • Includes variants associated with certain high-risk ancestral groups.



Fill out the form below and one of our specialists will be in touch.

(BETA) Choose a language to view this content in:
About the translation.