GITELMAN SYNDROME (SLC12A3) GENE SEQUENCING

A genetic test that identifies mutations in the SLC12A3 gene, responsible for Gitelman syndrome, a rare kidney disorder that affects salt and electrolyte balance.

Also known asGitelman Syndrome (slc12a3) Gene Sequencing Gitelman Syndrome (slc12a3) Gene Sequencing

Available via

Home Collection, Lab Visit

Contains

1 parameters

Earliest reports in

28 Working Days

Test details
Preparations

No special preparations needed

Test included
GITELMAN SYNDROME (SLC12A3) GENE SEQUENCING includes 1 parameter

  • Specimen

Test code

G685

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Others (fx)Others2 ML

Specimen stability information

Others (Fx)

Specimen rejection criteria

Test run frequency

Every Day TIME - 10:00

Turn around time

28 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

GITELMAN SYNDROME (SLC12A3) GENE SEQUENCING

22000