Empower Screening.
Hereditary Cancer Risk · Physician-Ordered Screening
A physician-ordered hereditary cancer screening analyzing 47+ genes linked to breast, ovarian, colorectal, pancreatic, and other inherited cancer syndromes. Results reviewed with a board-certified MD in person or via telehealth. Joint Commission-accredited facility, 9445 Harding Ave in Surfside.
What is Empower hereditary cancer screening?
What This Screening Detects.
Empower’s panel covers the most clinically actionable hereditary cancer genes recognized by NCCN guidelines. Below are the gene families and the cancers they influence.
Myriad Empower · by the numbers.
Empower is built on Myriad MyRisk, the most published hereditary-cancer panel in the United States with more than two decades of laboratory validation. Performance figures below come directly from Myriad’s technical specifications and peer-reviewed literature.
Cancer types & relevant genes.
A pathogenic variant in any of the genes below dramatically elevates lifetime risk for the corresponding cancer site. Identifying that variant earlier allows our physicians to build a personalized surveillance plan, recommend risk-reducing options, and offer cascade testing to first-degree relatives.
Breast & Ovarian (HBOC)
BRCA1, BRCA2, PALB2, CHEK2, ATM, BARD1, RAD51C, RAD51D
Hereditary Breast & Ovarian Cancer Syndrome — the most common indication for hereditary cancer testing, with lifetime breast-cancer risk reaching 70% in BRCA1 carriers.
Colorectal & Uterine (Lynch)
MLH1, MSH2, MSH6, PMS2, EPCAM
Lynch Syndrome — the leading cause of inherited colorectal cancer; carriers benefit from colonoscopy starting in the 20s and gynecologic surveillance.
Polyposis Syndromes
APC, MUTYH, STK11, SMAD4, BMPR1A
Familial Adenomatous Polyposis (APC), MUTYH-Associated Polyposis, Peutz-Jeghers, and Juvenile Polyposis Syndrome.
Pancreatic
BRCA1, BRCA2, PALB2, ATM, CDKN2A, STK11, MLH1
Pancreatic-cancer susceptibility genes overlap heavily with HBOC and Lynch — one reason a single multi-gene panel is more efficient than gene-by-gene testing.
Melanoma
CDKN2A, CDK4, BAP1
Familial atypical multiple-mole melanoma (FAMMM) syndrome — warrants enhanced dermatologic surveillance and ocular screening.
Li-Fraumeni / Cowden
TP53, PTEN
Multi-system cancer predisposition syndromes affecting breast, brain, soft-tissue, adrenal, thyroid, endometrium, and other sites.
Hereditary Diffuse Gastric
CDH1
CDH1-associated hereditary diffuse gastric cancer; carriers may consider risk-reducing total gastrectomy plus annual breast MRI.
Renal, Prostate, Endocrine
VHL, FH, MET, MEN1, RET, SDHx
von Hippel-Lindau, hereditary leiomyomatosis, hereditary papillary renal, MEN1, MEN2, and paraganglioma/pheochromocytoma syndromes.
What changes when we find something.
A positive Empower result is not a diagnosis — it is information. Acted on early, that information meaningfully reduces your future cancer risk through four pathways our physicians coordinate.
Enhanced Surveillance
Earlier and more frequent imaging — for example, annual breast MRI alternating with mammogram for BRCA carriers, or colonoscopy every 1–2 years starting at age 20–25 for Lynch carriers.
Risk-Reducing Options
Where appropriate and personally chosen, prophylactic surgery (mastectomy, salpingo-oophorectomy, gastrectomy) or chemoprevention can lower lifetime cancer risk by 90% or more.
Cascade Testing for Family
First-degree relatives have a 50% chance of carrying the same variant. Identifying the variant in one family member opens the door to focused, lower-cost testing for parents, siblings, and children.
NCCN-Aligned Care Plan
Our physicians follow National Comprehensive Cancer Network (NCCN) Guidelines ® for hereditary cancer management — the same evidence-based protocols used at major academic cancer centers.
Who qualifies? NCCN guidelines support hereditary cancer testing for anyone with a personal or family history of: breast cancer before age 50, ovarian or pancreatic cancer at any age, triple-negative breast cancer, male breast cancer, three or more relatives with the same or related cancers, Ashkenazi Jewish ancestry with any breast or ovarian cancer in the family, or a known pathogenic variant in a relative.
How It Works.
From consult to action plan, every step is physician-led.
Who Should Consider.
Hereditary cancer screening is appropriate for adults with personal or family histories that suggest an inherited risk pattern. Common indications include:
Why TrufaMED for Empower Hereditary Cancer Screening.
Why patients choose TrufaMED for Empower screening:
47+ hereditary cancer genes, physician-ordered and physician-reviewed.
Pricing & Coverage.
Insurance: Most major insurance plans cover Empower when NCCN clinical criteria are met (personal or family history, ancestry risk, prior cancer diagnosis). Our team verifies benefits and obtains prior authorization before the sample is collected.
Self-pay: Available for patients without coverage or who prefer not to use insurance. Call (305) 537-6396 for a current self-pay quote. Payment plans available.
What is included: Physician consult, test order, sample collection, lab analysis, results review visit, and coordinated genetic-counselor referral when indicated.
Physician-Led.
Every order, interpretation, and follow-up is delivered by a board-certified MD.
Visit Us in Surfside, FL.
Surfside, FL 33154
Frequently Asked Questions.
Does insurance cover Empower hereditary cancer screening?
Most major insurance plans cover Empower when NCCN clinical criteria are met, including a qualifying personal or family history of cancer. Our team verifies benefits and obtains prior authorization before any sample is collected. Coverage varies by plan, so we confirm in writing before proceeding.
What happens if I test positive for a BRCA1 or BRCA2 mutation?
A positive result indicates elevated lifetime risk, not a current cancer diagnosis. Your TrufaMED physician builds a risk-management plan that may include enhanced imaging surveillance (breast MRI, transvaginal ultrasound), risk-reducing medication, surgical risk reduction options, and coordinated referrals to oncology and genetic counseling. We also help organize cascade testing for first-degree relatives.
Do I need genetic counseling before or after testing?
Pre-test counseling can be performed by your TrufaMED physician for straightforward indications. Post-test counseling with a board-certified genetic counselor is strongly recommended for any positive result or variant of uncertain significance. We coordinate that referral.
How long until I get results?
Results typically return from Myriad in 2 to 3 weeks from the date the sample is received. We schedule your results visit as soon as the report is signed out.
What does a ‘variant of uncertain significance’ (VUS) result mean?
A VUS is a genetic change whose clinical impact is not yet established. It is not treated as a positive result and does not change clinical management. Variants are reclassified over time as more data accumulates, and we re-contact patients if a VUS is reclassified.
Is the sample blood or saliva?
Either, depending on the panel and patient preference. Most adults at our Surfside clinic provide a blood sample drawn by a licensed provider during the visit. Saliva kits are available for select circumstances.
Can I get tested if I have already had cancer?
Yes. In fact, many guidelines recommend germline testing for any patient with a personal history of breast, ovarian, pancreatic, colorectal, or prostate cancer, regardless of family history or age at diagnosis. Results may inform treatment decisions, surveillance for second cancers, and cascade testing for relatives.
Does my whole family need testing?
Not initially. The first step is testing the person most likely to carry a mutation, typically the family member with the youngest cancer diagnosis. Once a specific mutation is identified, single-site testing for relatives is much less expensive and almost always covered by insurance.
How is my genetic data protected?
Myriad is HIPAA-compliant and does not share identifiable data with third parties without consent. Federal law (GINA) prohibits employers and health insurers from using genetic test results to discriminate. GINA does not extend to life, disability, or long-term care insurance, which is something we discuss before testing.
Is there a difference between Empower and direct-to-consumer ancestry tests?
Yes, substantial. Direct-to-consumer ancestry tests typically genotype only a handful of common variants, often missing 90%+ of clinically actionable mutations. Empower uses full-gene sequencing plus large-rearrangement analysis, classified per ACMG criteria, with physician-grade reporting suitable for medical decision-making.
Can I be tested while pregnant?
Yes. Hereditary cancer testing is safe during pregnancy and is sometimes prioritized when a pregnant patient has a strong family history. We coordinate timing of any results-based interventions with your obstetrician.
What if I cannot make it to the Surfside clinic?
Telehealth consultations are available statewide for the consult and results visits. Sample collection requires either an in-person visit to our Surfside clinic or a saliva kit shipped to your residence.
Other TrufaMED Services.
Ready to get started?
Speak with a TrufaMED physician about whether empower hereditary cancer screening is appropriate for you.