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Alpha-1-Antitrypsin Phenotyping
Definitive analysis of hereditary a1-antitrypsin deficiency, which is associated with chronic obstructive pulmonary disease (COPD) (panacinar emphysema), hepatic cirrhosis, and hepatoma. Cholestasis with neonatal hepatitis is found in a minority of neonates with a1AT deficiency...
View Lab TestAPOE Alzheimer's Risk
This test is to detect the presence of the APOE4 variant, which is associated with increased risk of late-onset (age >60-65) Alzheimer's disease (AD). Testing may be considered for patients with dementia to supplement information from clinical and other evaluations. This test...
View Lab TestCardiometabolic Panel
Cardiometabolic PanelDesigned to help people understand why they are experiencing obesity, blood sugar dysregulation, insulin resistance, elevated cardiovascular markers, or lipid imbalances.TRAITS 8GENES 7SNPS 106Cardiometabolic disorders, including cardi...
View Lab TestCardiometabolic Panel (Add-on)
Cardiometabolic PanelDesigned to help people understand why they are experiencing obesity, blood sugar dysregulation, insulin resistance, elevated cardiovascular markers, or lipid imbalances.TRAITS 8GENES 7SNPS 106Cardiometabolic disorders, including cardi...
View Lab TestCognitive Panel
Cognitive PanelDesigned to support people who are experiencing anxiety, depression, inability to focus, loss of memory or have a history of head trauma.TRAITS 10GENES 104SNPS 155There are many conditions that can impact a client's cognitive health, i...
View Lab TestCognitive Panel (Add-on)
Cognitive PanelDesigned to support people who are experiencing anxiety, depression, inability to focus, loss of memory or have a history of head trauma.TRAITS 10GENES 104SNPS 155There are many conditions that can impact a client's cognitive health, i...
View Lab TestComprehensive Genetic Panel
This groundbreaking DNA health panel provides fast and accurate information on a wide range of SNP's (single nucleotide polymorphisms) affecting weight management, diabetes, cardiac heath, nutritional function, bone health and estrogen metabolism, memory and brain health, m...
View Lab TestCOMT
COMT (Val158Met) MutationCOMT is the gene's official symbol for the gene “catechol-O-methyltransferase”. The COMT gene provides instructions for making an enzyme called catechol-O-methyltransferase. Two versions of this enzyme are made from the gene. The longer...
View Lab TestCystic Fibrosis (CF) Profile, 32 Mutations, DNA Analysis
Help determine affected or carrier status for the 32 most common CF mutations.This assay detects as many as 90% of cystic fibrosis carriers in the Caucasian population. Within other ethnic groups, there may be higher or lower detection efficiency. Includes the mutation profile...
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