Germline confirmation service following Haematology genomic testing

Single gene testing for potentially inherited variants following detection in Haematology gene panel.

Test description

Identifying an inherited variant aids in the diagnosis and management of the patient and their family members.

Test information

Test name

Germline confirmation test

Clinical indication

For determination of whether a somatic variant in a blood cancer is inherited.

Gene(s)

One or more of the genes found in the Haematology NGS panel.

Method

Next generation sequencing

Turn around time

3 weeks

Medicare eligibility

No

Price

$475. Where Genomic Diagnostics has identified a DDX41 potential germline variant, testing is free of charge as part of the service.

Test request form

Haematology genetics test request form preferred. Standard pathology request form accepted.

Sample type

Hair follicles

Collection type

Patient to collect

Special instructions

FAQ

No items found.

Resources

No items found.