Fanconi Anemia Report

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

The Fanconi Anemia Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Fanconi Anemia instead of a limited set of genes, like old genetic target panels.

Fanconi anemia is a condition that affects many parts of the body. People with this condition may have bone marrow failure, physical abnormalities, organ defects, and an increased risk of certain cancers.

Along with environmental factors, Genetics plays a key role in the regulation of Fanconi Anemia.

• 22 genes analyzed
• 100% genomic regions covered
• Intragenic and intergenic regions analyzed
• All variants reported

List of genes:

ATM,ATR,BLM,BRCA2,BRIP1,CXCR4,ERCC4,FANCA,FANCB,FANCC,FANCD2,
FANCE,FANCF,FANCG,FANCI,FANCL,FANCM,NBN,PALB2,RAD51C,SLX4,
XRCC2