SCN1B Sequencing

Mutations in the SCN1B gene cause a spectrum of seizure disorders, ranging from early-onset isolated febrile seizures to generalized epilepsy with febrile seizures plus (GEFS+). This laboratory performs Sanger sequencing of the SCN1B gene.

Forms & Docs

Ordering

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Test Code
S0093

Turn Around Time
2-3 weeks

Billing

CPT Code
81404×1

Ordering Guidance

If there are questions regarding this test, please contact Client Services at 617-553-5880 or clientservices@claritasgenomics.com

Details

Genes Covered
SCN1B

Methods
Sanger