The Epilepsy Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Epilepsy instead of a limited set of genes, like old genetic target panels.
Epilepsy is a central nervous system (neurological) disorder in which brain activity becomes abnormal, causing seizures or periods of unusual behavior, sensations, and sometimes loss of awareness.
Along with environmental factors, Genetics plays a key role in the regulation of Epilepsy.
- 534 genes analyzed
- 100% genomic regions covered
- Intragenic and intergenic regions analyzed
- All variants reported