Renasight™ Key highlight
Comprehensive Panel, Custom-Designed for Nephrology
Carefully curated analysis of 397 genes using Next-Generation Sequencing (NGS) technology.
Identifies recessive, and X-linked autosomal recessive, and X-linked disorders, as well as the APOL1 risk allele
Panel-wide single-nucleotide variant (SNV) and copy-number variant (CNV) detection
Reports out pathogenic and likely pathogenic variants hand-selected by genetic experts to provide actionable information
Results available in ~3 weeks
International Standards: Samples are sent for examination at an American laboratory with ISO 15189/15190 standards and CAP