Wellness Testing
Clinical grade testing to inform health screening and maintenance
Predictive genetic screening offers healthy individuals a clinical-grade genetic test to screen for genetic variants that increase risks of certain conditions. Our Genomic Inform® testing can help your patients understand what risks, if any, they may have.
Up to 15% of generally healthy adults have at least one genetic finding that raises their risks for a treatable or preventable condition.1 Learning about a genetic risk better informs medical screening and important interventions.
Our whole genome analysis approach
We use a comprehensive, whole genome analysis approach to identify risks from conditions that can occur across the lifespan. Our Genomic Inform® testing is unlike any healthy genetic screening test available, using a genome-wide and systematic method to identify nearly all manner of risk variants.
Sequence variants analysis
including single nucleotide variants, deletions/insertions, intronic, and regulatory variants
Structural & copy number variants
including duplications, deletions, regions of homozygosity, mobile element insertions, inversions, and aneuploidy
Short tandem repeats for selected genes
in >25 genes
Mitochondrial variants
with heteroplasmy and large deletions
Learn about risks across multiple areas of health
Cancer conditions
Heart conditions
Neurological disorders
Bleeding disorders
Metabolic disorders
Carrier findings in over 600 genes
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Genomic Inform® testing
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Documents needed for testing
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