Porphyria Panel
Porphyria Panel
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The genetic variants analyzed in this panel are closely related to or, potentially, the cause of the major porphyria 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
- 10 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Cutaneous porphyria
- Variegate porphyria
- Acute intermittent porphyria
- X-linked erythropoietic protoporphyria
List of genes analyzed:
ALAD, ALAS2, CLPX, CPOX, FECH, HFE, HMBS, PPOX, UROD, UROS

Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.