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Results: 1 to 20 of 39 (representing 18 labs)

Tests names and labsConditionsGenes and analytesMethods

Parkinsons disease panel

Centogene AG - the Rare Disease Company
Germany
2830
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

PARK1 Parkinsonism

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Parkinson’s Disease via the SNCA Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Parkinson Disease Sequencing Panel

PreventionGenetics
United States
1716
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SNCA. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

SNCA. MLPA testing

Instituto de Medicina Genomica
Spain
11
  • D Deletion/duplication analysis

SNCA. MLPA testing

Instituto de Medicina Genomica
Spain
11
  • D Deletion/duplication analysis

SNCA. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Parkinson Disease , Deletions-Duplications (MLPA) SNCA, PARK2, PINK1, PARK7, LRRK2, UCHL1 Genes

Reference Laboratory Genetics
Spain
66
  • D Deletion/duplication analysis

Parkinson Disease Type 1, Sequencing Exons (3-4) SNCA (PARK1) Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Invitae Combined Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel

Invitae
United States
4721
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SNCA Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • C Sequence analysis of the entire coding region

Invitae Hereditary Parkinson's Disease and Parkinsonism Panel

Invitae
United States
1815
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PARKINSON DISEASE

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1010
  • C Sequence analysis of the entire coding region

Parkinson disease 1: SNCA (PARK1) gene deletions-duplications analysis (MLPA)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • D Deletion/duplication analysis

Parkinson Disease

Asper Biogene Asper Biogene LLC
Estonia
1716
  • C Sequence analysis of the entire coding region

NGS panel - dementia

Genome Diagnostics VU University Medical Center
Netherlands
2341
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

NGS panel - Parkinson

Genome Diagnostics VU University Medical Center
Netherlands
2036
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

SNCA(PARK1) - Gene Sequencing & Del/Dup analysis

Genome Diagnostics VU University Medical Center
Netherlands
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • T Targeted variant analysis

Results: 1 to 20 of 39

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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