For general topics, click here.

Renal Testing Service FAQs

Q: Why does my test result take so long?
A: DNA sequencing is inherently a time-consuming process. In addition, the genes for the renal diseases currently available for analysis are generally quite large. For example, the analysis of PKD1 and PKD2 genes for Athena’s PKDx™ analysis requires sequencing of more DNA than any other currently available commercial clinical diagnostic testing service.

Q: Will my test be covered by insurance?
A: The answer to this very much depends on the patient’s individual coverage, deductibles, etc. In general, however, our experience is that there is good reimbursement for our tests. Please feel free to contact one of our Patient Advocates to discuss your individual situation.

PKDx™ Family Testing Service FAQs

Q: I have a patient that has clear PKD based on clinical symptoms. I’d like to test his brother as a potential donor. Can I use the Family Testing Service for the brother?
A: No. Athena only provides the single amplicon (Family Testing) service to patients for whom the familial mutation has already been identified. If you would like to have the recipient tested, please contact client services to arrange for testing

Q: There is more than one alteration listed on the result report for the proband. Can I have just those segments tested in the relative?
A: Yes. Athena will test up to three (3) segments in the relative at no additional cost.

Q: What is the cost of testing a relative?
A: The price for each relative is $495.00. Athena will test up to three (3) segments in each relative at no additional cost.