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Gilbert Syndrome Panel

Gilbert Syndrome Panel

Prix habituel €29.00 EUR
Prix habituel Prix soldé €29.00 EUR
Vente Épuisé
This product is only meant for customers who already purchased a MyGenome Test

The Gilbert Syndrome panel is a genetic test used to identify mutations in the UGT1A1 gene, which is involved in bilirubin metabolism. Mutations in this gene can lead to Gilbert syndrome, a common genetic disorder characterized by elevated levels of bilirubin in the blood. The panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of Gilbert syndrome or individuals with symptoms of the condition, such as mild jaundice, fatigue, and abdominal pain. Genetic testing can confirm a diagnosis, inform treatment and management decisions, and guide family planning. Testing can also provide reassurance for unaffected family members.

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
  • 1 or more genes analyzed
  • Investigates SNP and Indel mutations up to 150 bp

List of main conditions:
  • Gilbert Syndrome
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Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.