FG Syndrome, FGS1 (MED12) R961W Mutation : ARUP Lab Tests

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FG Syndrome, FGS1 (MED12) R961W Mutation : 0051752

Patient History for FG Syndrome

Mnemonic: FGS 1

Methodology:	Polymerase Chain Reaction/Fluorescence Monitoring
Performed:	Tue
Reported:	7-10 days
Specimen Required:	Collect: Lavender (EDTA), pink (K₂EDTA), or yellow (ACD Solution A or B). Specimen Preparation: Transport 3 mL whole blood. (Min: 1 mL) Storage/Transport Temperature: Refrigerated. Stability (collection to initiation of testing): Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable

Interpretive Data:	Refer to report. Counseling and informed consent are recommended for genetic testing. Consent forms are available online at www.aruplab.com. Refer to Statement C under Testing Information at http://www.aruplab.com.
CPT Code(s):	83891 Isolation; 83898 Amplification; 83896 x 2 Nucleic acid probes; 83912 Interpretation and report - Additional CPT code modifiers may be required for procedure performed to test oncologic or inherited disorders.
Cross References:	MED12 (R961W) ( FG Syndrome, FGS1 (MED12) R961W Mutation) , Opits-Kaveggia Syndrome ( FG Syndrome, FGS1 (MED12) R961W Mutation)

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