Methylation Mechanisms Panel
Methylation Mechanisms Panel
Prix habituel
€29.00 EUR
Prix habituel
Prix soldé
€29.00 EUR
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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
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
List of main conditions:
List of genes analyzed:
AHCY, ASH1L, ASXL1, BHMT, BUD23, CBS, COMT, DNMT1, DNMT3A, DNMT3B, DOT1L, EBF3, EZH2, GATAD2B, GNMT, HNMT, KDM6B, KMT2C, KMT2D, MAT1A, MBD5, MECP2, MTHFR, MTRR, NDUFAF7, NSD1, NSD3, NSUN2, PHF8, PRMT7, SETD2, SHMT1, SMCHD1, TET1, TFB1M, TRMT1, TRMT5, ZFP57
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The genetic variants analyzed in this panel are closely related to or, potentially, the cause of major methylation mechanism 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
- 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
List of genes analyzed:
AHCY, ASH1L, ASXL1, BHMT, BUD23, CBS, COMT, DNMT1, DNMT3A, DNMT3B, DOT1L, EBF3, EZH2, GATAD2B, GNMT, HNMT, KDM6B, KMT2C, KMT2D, MAT1A, MBD5, MECP2, MTHFR, MTRR, NDUFAF7, NSD1, NSD3, NSUN2, PHF8, PRMT7, SETD2, SHMT1, SMCHD1, TET1, TFB1M, TRMT1, TRMT5, ZFP57
Ce produit est uniquement destiné aux clients qui ont déjà acheté un test MyGenome.