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Marfan Syndrome Panel

Marfan Syndrome Panel

Regular price €49.00 EUR
Regular price Sale price €49.00 EUR
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This product is only meant for customers who already purchased a MyGenome Test

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
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This product is only meant for customers who already purchased a MyGenome Test