Quest Diagnostics Nichols Institute

Project ID

1503

Facility Name

Analyte

vascular disease (prothrombin G20210A, Factor V HR2 variant (A4070G),MTHFR C677T/A1298C) susceptibility mutation panel

Method

PCR/OLA/Tag-It Luminex

Specimen Type

whole blood; amplicons: DNA

Permit Category

Genetic Testing - Molecular

Status

Approved

Facility State

Facility ID

2478