PreSENTIA: Familial Melanoma

Synonyms: -

Material:

Buccal swab

TAT:

2-3 weeks

Method:

NGS

Overview

Familial melanoma is an inherited condition which can lead to the formation of melanoma, a type of skin cancer, in the future. Mutated genes that lead to familial melanoma can run in families and pass from generation to generation. Patients with familial melanoma have higher risk of early development of melanomas as well as develop multiple primary melanomas.

PreSENTIA Familial Melanoma cancer panel tests for numerous germline mutations in 7 genes that could cause familial melanoma skin cancers in the future. Identifying germline mutations associated with cancer susceptibility empowers healthcare providers and patients, as it allows them to take better and more informed decisions.

PreSENTIA: Familial Melanoma

7 Gene(s)*

BAP1

BRCA2

CDK4

CDKN2A

PTEN

RB1

TP53

Who is the test for

How many hereditary cancer syndromes are associated with this panel

Recommendations by professional bodies

References

Created by

Our editorial team consists of medical specialists and scientists in the field of human genetics. All content is created and reviewed in accordance with current scientific standards.

Last Update : 01.10.2026

How to order a genetic test

Select the right test for your patients. Contact our team in case you do not have an active contract yet.

Collect the sample. Download and fill in the order and consent form or access our portal (available for sample sent to Germany).

Properly pack the sample and send it to Medicover Genetics.

The sample will be analysed in our accredited laboratories.

An actionable report will be available for you to access safely and securely.

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