Cowden Syndrome Panel
Cowden Syndrome Panel
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€29.00 EUR
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€29.00 EUR
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"This product is only meant for customers who already purchased a MyGenome Test
A rare inherited disorder characterized by the presence of many benign (non-cancerous) growths called hamartomas and an increased risk of cancer. Hamartomas form in different parts of the body, especially the skin, mouth and gastrointestinal tract.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
List of genes analyzed:
AKT1, KLLN, PIK3CA, PTEN, SDHB, SDHC, SDHD, SEC23B"
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A rare inherited disorder characterized by the presence of many benign (non-cancerous) growths called hamartomas and an increased risk of cancer. Hamartomas form in different parts of the body, especially the skin, mouth and gastrointestinal tract.
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
- 8 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Cowden Syndrome
List of genes analyzed:
AKT1, KLLN, PIK3CA, PTEN, SDHB, SDHC, SDHD, SEC23B"
This product is only meant for customers who already purchased a MyGenome Test