Marfan Syndrome Panel
Marfan Syndrome Panel
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Marfan syndrome is a genetic condition that affects the connective tissue, which provides support to the body and organs. Marfan syndrome can damage blood vessels, the heart, eyes, skin, lungs, and bones in the hips, spine, feet, and rib cage.
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 25 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Marfan Syndrome
List of genes analyzed:
ABL1, ADAMTS10, ADAMTS17, ADAMTSL4, BGN, CBS, COL11A1, COL11A2, COL1A1, COL1A2, COL2A1, COL3A1, COL5A1, COL5A2, EFEMP2, FBN1, FBN2, MAT2A, MED12, PLOD1, SKI, SLC2A10, SMAD3, SMAD6, TGFB2, TGFB3, TGFBR1, TGFBR2, UPF3B, VCAN

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