Methylation Mechanisms Panel
Methylation Mechanisms Panel
Prix habituel
€29.00 EUR
Prix habituel
Prix soldé
€29.00 EUR
Prix unitaire
par
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This product is only meant for customers who already purchased a MyGenome Test
The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major methylation mechanism conditions
Methylation mechanisms panel is used to identify genetic variants associated with methylation disorders, a group of rare genetic disorders that affect DNA methylation, a chemical modification that regulates gene expression. Methylation disorders are caused by mutations in genes involved in DNA methylation and demethylation, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of methylation disorders or individuals with symptoms of the conditions, such as developmental delay, intellectual disability, and immune dysfunction. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and 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.
List of main conditions:
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The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major methylation mechanism conditions
Methylation mechanisms panel is used to identify genetic variants associated with methylation disorders, a group of rare genetic disorders that affect DNA methylation, a chemical modification that regulates gene expression. Methylation disorders are caused by mutations in genes involved in DNA methylation and demethylation, and this panel tests for genetic variants that are known to affect these processes.
This panel is designed for individuals with a family history of methylation disorders or individuals with symptoms of the conditions, such as developmental delay, intellectual disability, and immune dysfunction. Genetic testing can confirm a diagnosis, provide information on disease severity and progression, and inform treatment and management decisions. Testing can also inform family planning decisions and 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
- More than 35 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Methionine Adenosyltransferase Deficiency
- Glycine N-Methyltransferase Deficiency
- Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.