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Results: 1 to 20 of 29

Tests names and labsConditionsGenes and analytesMethods

Gitelman syndrome

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

Bartter syndrome

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

ExomePLUS Electrolyte & KidneyStone

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
4649
  • C Sequence analysis of the entire coding region

KidneySeq: A Comprehensive Inherited Kidney Disease Panel

Iowa Institute of Human Genetics University of Iowa
United States
122147
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15391578
  • C Sequence analysis of the entire coding region

SLC12A3. Complete sequencing

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

Gitelman syndrome via the SLC12A3 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

BARTTER SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2927
  • C Sequence analysis of the entire coding region

Gitelman syndrome

Institute of Human Genetics Cologne University
Germany
11
  • C Sequence analysis of the entire coding region

CarrierMap

Recombine
United States
299297
  • T Targeted variant analysis

Gitelman syndrome

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Gitelman syndrome (analysis of deletion/duplication of SLC12A3 gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

Gitelman syndrome (sequence analysis of SLC12A3 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Single gene testing SLC12A3

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

SLC12A3 Sequencing

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Gitelman syndrome, SLC12A3 sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

qChip

Quantitative Genomic Medicine Laboratories, SL
Spain
183162
  • D Deletion/duplication analysis

SLC12A3

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

Hereditary Renal Tubular Disorders Evaluation

Athena Diagnostics Inc Quest Diagnostics
United States
65
  • C Sequence analysis of the entire coding region

SLC12A3 DNA Sequencing Test

Athena Diagnostics Inc Quest Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.