WERNER SYNDROME (WRN) GENE SEQUENCING

A genetic test to identify mutations in the WRN gene, associated with Werner syndrome, a rare genetic disorder characterized by accelerated aging, early onset of age-related diseases, and a higher risk of cancer.

Also known asWerner Syndrome (wrn) Gene Sequencing Werner Syndrome (wrn) 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
WERNER SYNDROME (WRN) GENE SEQUENCING includes 1 parameter

  • Specimen

Test code

G679

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

WERNER SYNDROME (WRN) GENE SEQUENCING

22000