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Genetic Testing & Molecular Diagnostics
Medicare Part B Covered ($0 Copay)PANEL-MET-16

Metabolic & Monogenic Diabetes Panel

Up to 5% of patients diagnosed with Type 2 diabetes actually have Monogenic Diabetes (MODY), an inherited single-gene disorder. Correct genetic classification can allow patients to transition from daily insulin injections to simple, well-tolerated oral sulfonylurea tablets, dramatically improving blood sugar control and quality of life.

Metabolic Genes16 Biomarkers
Diagnostic ImpactMedication Shift
Medicare Out-of-Pocket$0.00
Accuracy99.9%

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

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Who Should Consider This Screening?

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

Diabetes diagnosed at a younger age (<35 years) with normal body mass index (BMI).
Diabetes spanning three consecutive generations in the family lineage.
Absence of typical Type 2 diabetes characteristics (no obesity, normal lipid profile).
Negative pancreatic islet autoantibodies (ruling out classic Type 1 diabetes).
Mild, persistent fasting elevated blood sugar that remains stable over decades.

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
HNF1A & HNF4AHepatocyte Nuclear Factor 1 & 4 Alpha (MODY 3 & 1)Regulates pancreatic beta-cell insulin secretion response to glucose.Allows clinical transition from insulin to low-dose oral sulfonylureas with superior glycemic control.
GCKGlucokinase Pancreatic Glucose Sensor (MODY 2)Controls the baseline fasting glucose threshold in liver and pancreas.Confirms benign, stable mild hyperglycemia that typically requires zero medication, avoiding overtreatment.
PPARG & KCNJ11Insulin Sensitivity & Potassium Channel SubunitsModulates peripheral insulin resistance and neonatal/atypical diabetes pathogenesis.Directs personalized selection of GLP-1, SGLT-2, or oral hypoglycemic medication classes.

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 ClassificationPathogenic Variant Identified
Identified Finding:

Heterozygous pathogenic mutation identified in HNF1A (c.872dupC, p.Pro291fs) confirming MODY 3.

Clinician Recommendation:

Discuss with endocrinologist for potential transition from insulin therapy to oral low-dose glimepiride/gliclazide with continuous glucose monitoring.

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 monogenic diabetes genetic testing when ordered by an attending physician to clarify diagnosis and tailor pharmacological management.

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 Metabolic & Monogenic Diabetes Panel?

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

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