Hereditary Cancer Panel
Hereditary Cancer Panel
Prix habituel
€29.00 EUR
Prix habituel
Prix soldé
€29.00 EUR
Prix unitaire
par
Impossible de charger la disponibilité du service de retrait
This product is only meant for customers who already purchased a MyGenome Test
The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major oncological conditions
Hereditary cancer panel is used to identify genetic variants associated with an increased risk of developing certain types of cancer, such as breast cancer, ovarian cancer, and colon cancer. This panel tests for genetic variants that are known to affect tumor suppressor genes and DNA repair pathways.
This panel is designed for individuals with a family history of cancer or individuals who have been diagnosed with cancer at a young age. Genetic testing can provide information on disease risk and severity, as well as inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
Afficher tous les détails
The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major oncological conditions
Hereditary cancer panel is used to identify genetic variants associated with an increased risk of developing certain types of cancer, such as breast cancer, ovarian cancer, and colon cancer. This panel tests for genetic variants that are known to affect tumor suppressor genes and DNA repair pathways.
This panel is designed for individuals with a family history of cancer or individuals who have been diagnosed with cancer at a young age. Genetic testing can provide information on disease risk and severity, as well as inform treatment and management decisions. Testing can also inform family planning decisions and provide reassurance for unaffected family members.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 380 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Hereditary breast ovarian cancer syndrome
- Neurofibromatosis
- Intraocular Retinoblastoma
- Familial adenomatous polyposis
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.