The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major gastroenterological conditions
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
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.