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Results: 1 to 14 of 14

Tests names and labsConditionsGenes, analytes, and microbesMethods

Precision HealthPGx Panel (25 Genes)

RPRD Diagnostics, LLC
United States
9723
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Admera Health PGxOne™ Plus

Admera Health
United States
993
  • T Targeted variant analysis

Whole Pharmacogenomics Scan

RPRD Diagnostics, LLC
United States
10769
  • D Deletion/duplication analysis
  • T Targeted variant analysis

GLOBALpgx

Eugenomic S.L.
Spain
14521
  • T Targeted variant analysis

Pharmacogenomics SNaP-Shot

Ariel Precision Medicine
United States
126
  • T Targeted variant analysis

Polypharmacy Comprehensive Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
3324
  • D Deletion/duplication analysis
  • T Targeted variant analysis

[Acetylation, slow], 243400, Autosomal recessive (NAT2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Genomic Unity® Pharmacogenomics Analysis

Variantyx, Inc.
United States
113
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

PGS.pharma

MVZ diagnosticum Frankfurt MVZ diagnosticum GmbH
Germany
1812
  • T Targeted variant analysis

Slow acetylator due to N-acetyltransferase enzyme variant

Labor Dr. Wisplinghoff
Germany
11
  • T Targeted variant analysis

Pharmacogenetic panel

MVZ diagnosticum Frankfurt MVZ diagnosticum GmbH
Germany
4629
  • T Targeted variant analysis

NAT2

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

NAT2 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 14 of 14

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.