Porphyria Report

 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