Gastroenterology Panel
Gastroenterology Panel
Regular price
$29.00 USD
Regular price
Sale price
$29.00 USD
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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 gastroenterological conditions
Gastroenterology panel is used to identify genetic variants associated with a range of gastrointestinal disorders, including inflammatory bowel disease, celiac disease, and other conditions affecting the digestive system. This panel tests for genetic variants that are known to affect immune function and inflammation, as well as genes involved in the metabolism of nutrients and drugs.
This panel is designed for individuals with a family history of gastrointestinal disorders or individuals with symptoms of the conditions, such as abdominal pain, diarrhea, or malabsorption. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform lifestyle modifications, such as changes to diet and exercise habits.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
See more about the product
The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major gastroenterological conditions
Gastroenterology panel is used to identify genetic variants associated with a range of gastrointestinal disorders, including inflammatory bowel disease, celiac disease, and other conditions affecting the digestive system. This panel tests for genetic variants that are known to affect immune function and inflammation, as well as genes involved in the metabolism of nutrients and drugs.
This panel is designed for individuals with a family history of gastrointestinal disorders or individuals with symptoms of the conditions, such as abdominal pain, diarrhea, or malabsorption. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform lifestyle modifications, such as changes to diet and exercise habits.
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 145 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Lactase Deficiency, Congenital
- Pancreatitis, Hereditary
- Congenital Short Bowel Syndrome

This product is only meant for customers who already purchased a MyGenome Test
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