Explore our tests
Discover the right genetic test for your patient in our complete list of tests and panels.
Showing 10 out of 408 tests
Pantothenate Kinase-Associated Neurodegeneration (PKAN, Hallervorden-Spatz Disease) via the PANK2 Gene
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 8347
1 Gene
Parkinson Disease and Parkinsonism Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10623
70 Genes
Parkinson Disease Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10337
24 Genes
Parkinson Disease via the LRRK2 Gene
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 11457
1 Gene
Paroxysmal Paralytic Rhabdomyolysis via the LPIN1 Gene, Exons 18-19 Deletion
Targeted PCR
2 - 3 weeks (8 - 10 days STAT)•Test 319
1 Gene
Pediatric Cataracts Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10413
41 Genes
Pendred Syndrome and Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10051
3 Genes
Periodic Fever Syndromes Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (6 - 12 days STAT)•Test 10315
13 Genes
Peroxisomal Biogenesis Disorder-Zellweger Spectrum Disorder (PBD-ZSD) Sponsored Testing Program
Sponsored TestNGS with CNV (Exome or Genome Platform)
2 - 3 weeks•Test 12655
13 Genes
Peroxisomal Disorders Panel
NGS with CNV (Exome or Genome Platform)
2 - 3 weeks (7 - 16 days STAT)•Test 10369
27 Genes