Systemic mastocytosis Panel
Systemic mastocytosis Panel
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The genetic variants analyzed in this panel are closely related to or potentially the cause of sistemic mastocustosis conditions
Systemic mastocytosis is a rare disorder that affects the body's mast cells, leading to symptoms such as skin rash, abdominal pain, and anaphylaxis. Systemic mastocytosis is caused by mutations in genes involved in the regulation of mast cells, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of systemic mastocytosis or individuals with symptoms of the condition, such as skin rash, abdominal pain, and anaphylaxis. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and 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 5 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Myelodysplastic Syndrome
- Systemic Mastocytosis With Associated Hematologic Neoplasm
- Diffuse Cutaneous Mastocytosis

What You Get
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Wellness Report
See a reportThe Wellness Report clarifies which habits are best suited to your genome, with actionable insights to live a better life.
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Scientific Fitness Report
See a reportThe Fitness report gives you actionable advice on training, sports, fitness and physical activity. This will help you develop the right workout for you based on your whole genome.
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Nutrigenomics Report
See a reportLearn about the relationships between food groups and your genes. Using this report, you can create the most effective and personalized diet with a specialist.
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Health and Predispositions
See the reportLearn more about your risk to develop +50 diseases and conditions. Start taking a proactive approach to your health with our actionable insights.
How it works
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Using a simple at home blood sample, we can collect the 100% of your DNA and analyze the genetic sequence in our lab.
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The sequence is divided into several parts, amplified, grouped in clusters and then sequenced.
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This sequencing process reveals the order of nucleotides that make up the original DNA sample.
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We then compare the genome with a generic and globally recognized reference DNA sequence.

Simple Blood Sample Collection
Painless, quick at home sample collection. User friendly device with CE-IVD mark and FDA approval.
Simply follow the packaging instructions and send the sample back using the pre-paid returns label.
Genomic Consultation Service
Would you like to speak with a genetic specialist? Book an individual session.
Our extensive network of geneticists will provide you with specialized genetic counseling on the topics that are most relevant for you such as diet and nutrition, fitness, injuries and many more.
Additional reports
Check out the full range of our additional reports, available upon completion of the Genome Test.