CAP & CLIA Accredited • Medicare Partner
Senior Wellness Care logo
Senior Wellness Care name
Genetic Testing & Molecular Diagnostics
Medicare Part B Covered ($0 Copay)PANEL-NCG-14

Neurocognitive & Dementia Genetics Panel

The Neurocognitive and Neurological Panel analyzes established genetic markers linked to late-onset memory impairment, cerebral amyloid deposition, and neurodegenerative conditions. Early identification allows healthcare providers to implement evidence-based neuroprotective interventions, vascular health monitoring, and personalized cognitive wellness plans years before clinical symptoms progress.

Key Markers TestedAPOE & 12 Genes
Clinical Accuracy99.9%
Medicare CoveragePart B Eligible
At-Home Process100% Painless

Check If You Qualify

Takes under 2 minutes • 100% Covered under Medicare Part B

Verify $0 Eligibility →
HIPAA 256-Bit Encrypted

Who Should Consider This Screening?

Healthcare providers recommend this diagnostic panel for individuals with the following personal or family health indicators:

Personal concerns regarding memory lapses, brain fog, or cognitive slowdown.
Immediate family member diagnosed with Alzheimer’s, vascular dementia, or Parkinson’s disease.
Co-occurring cardiovascular risk factors (hypertension, high homocysteine) impacting cerebral blood flow.
Patients over 65 seeking baseline neurocognitive risk assessments.

Biomarkers & Genes Evaluated in this Panel

Processed using high-complexity Next-Generation Sequencing (NGS) in CLIA-certified and CAP-accredited partner laboratories.

Gene Symbol / NameClinical SignificanceActionable Impact
APOE (e2 / e3 / e4 alleles)Apolipoprotein E Allelic GenotypingThe strongest established genetic susceptibility marker for late-onset sporadic cognitive decline.Informs early lifestyle, vascular risk management, sleep hygiene, and specialized neurological baseline testing.
PSEN1 & PSEN2Presenilin 1 & 2 Catalytic SubunitsRegulates amyloid precursor protein (APP) processing and gamma-secretase activity.Distinguishes early-onset familial variants from age-related memory vulnerabilities.
MAPT & GRNMicrotubule-Associated Protein Tau & ProgranulinAssociated with frontotemporal lobar degeneration and tauopathy pathways.Assists clinicians in differential diagnosis of atypical neurological and movement symptoms.

Sample Report & Diagnostic Action Plan

Every patient receives an easy-to-understand diagnostic summary and a detailed clinical report tailored for their primary care doctor.

Sample Result ClassificationModerate Risk Factor
Identified Finding:

APOE Genotype: e3/e4 (Heterozygous for the e4 susceptibility allele).

Clinician Recommendation:

Recommend annual Montreal Cognitive Assessment (MoCA), intensive management of cardiovascular lipids/blood pressure, and antioxidant-rich Mediterranean dietary protocol.

Medicare Part B Coverage Guidelines

Understand how federal CMS medical necessity guidelines apply to this specific diagnostic screening:

Covered 100% When Medically Necessary

Medicare Part B covers diagnostic neurological screening when ordered by a licensed physician in the context of cognitive evaluations, memory loss symptoms, or hereditary neurodegenerative family history.

Our network of state-licensed physicians reviews your medical profile to confirm eligibility before any kit is mailed.
$0 Out-of-Pocket for Qualifying Seniors

Ready to Check Your Eligibility for Neurocognitive & Dementia Genetics Panel?

Takes under 2 minutes • Painless at-home cheek swab • 100% Physician Reviewed

Start 2-Minute Pre-Qualification →