HAX1 Sequencing

Mutations in HAX1 result in severe congenital neutropenia/Kostmann disease, which are disorders of hematopoiesis. There are several types. This particular type is inherited in an autosomal recessive manner.

This laboratory performs Sanger sequencing of the HAX1 gene.

Forms & Docs

Ordering

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Test Code
S0864

Turn Around Time
3-5 weeks

Billing

CPT Code
81479×1

Ordering Guidance

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

Details

Genes Covered
HAX1

Methods
Sanger