This product is only meant for customers who already
purchased a Sequencing Test
The Porphyria Report is based on the Whole Genome Sequencing Test. As such, it analyses all Common and Rare Variants associated with Porphyria instead of a limited set of genes.
Porphyria is a group of disorders caused by abnormalities in the chemical steps that lead to heme production.
Along with environmental factors, Genetics plays a key role in the regulation of Porphyria.
- 9 genes analyzed
- 100% genomic regions covered
- Intragenic and intergenic regions analyzed
- All variants reported
List of genes:
ALAS2, CLPX, CPOX, FECH, HFE, HMBS, PPOX, UROD, UROS