Lucence CardioHemeRISK
See whether acquired blood-cell mutations add context to your heart attack, stroke, and leukemia risk.
- No doctor visit or referral needed
- Members pay our cost on every test, never a markup
- Tracked over time alongside your other results
- HSA/FSA eligible
- Typical results in about 12 working days · Reviewed by a real clinician
- Drawn at a CLIA/CAP-accredited lab near you · Find labs
Why people order the Lucence CardioHemeRISK
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Risk context beyond cholesterol
This test examines acquired blood-cell mutations, which answer a different question from lipid markers, blood pressure, or inherited-risk testing.
Who may consider the Lucence CardioHemeRISK
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Age-related risk context
Clonal hematopoiesis becomes more common with age. Age 40 and above is a recommendation, not a requirement, and being under 40 is not automatically disqualifying.
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Personal or family history
A history of early cardiovascular events or blood cancer may make an additional risk-assessment conversation useful, but this test does not diagnose either condition.
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Clinician-guided risk assessment
A clinician can interpret a detected clone alongside standard cardiovascular and hematology evaluation and decide whether follow-up is appropriate.
Is this the right test if I want a standard cardiovascular risk assessment?
No. Choose standard cardiovascular evaluation first, including blood pressure and lipid assessment. CardioHemeRISK may add a different layer of acquired-mutation context, but it does not replace those tests.
Should I choose this instead of inherited heart or cancer genetic testing?
No. CardioHemeRISK looks for acquired mutations in blood-forming cells, not variants you were born with. Choose germline testing only through an appropriate inherited-risk pathway.
Can I consider this test if I am under 40?
Yes, being under 40 is not automatically disqualifying. Age 40 and above is a recommendation, so discuss your history and goals with a clinician before deciding.
Is this appropriate if I have symptoms or a suspected blood disorder?
Do not use this screen to evaluate urgent symptoms or replace a diagnostic workup. Seek clinician-directed testing, especially for chest pain, stroke symptoms, unexplained blood-count changes, or other concerning findings.
Where is this test available?
This test is not available in Pennsylvania, New York, or Rhode Island.
How should I prepare for the blood draw?
Fasting is not required. Avoid a heavy meal before your draw. Have your blood drawn in the comfort of your home at no additional cost. Tell your care team about recent surgery, blood transfusion, or bone marrow transplant so they can confirm timing and eligibility.
What members say on Trustpilot
What the Lucence CardioHemeRISK measures
CardioHemeRISK is a blood-based next-generation sequencing risk assessment for clonal hematopoiesis, the expansion of blood-forming cell clones that carry acquired mutations. It examines ASXL1, CALR, DNMT3A, FLT3, IDH1, IDH2, JAK2, MPL, PPM1D, RUNX1, SF3B1, SRSF2, TET2, TP53, and U2AF1. The shared clonal signal is used to add context to heart attack, stroke, and leukemia risk.
These mutations are acquired during life, not inherited germline variants. The test is also different from cholesterol, lipoprotein, blood-pressure, imaging, and blood-count testing. It is a risk-assessment aid, not a diagnosis or a prediction that an event will occur, and it does not replace standard cardiovascular or hematology assessment.
- Specimen
- Blood sample
- Biomarker count
- 0 biomarkers
- Fasting
- Not required
- Results
- On your Mito dashboard in about 12 working days, with your range explained
Your results
How to understand your Lucence CardioHemeRISK result
Interpret the report with a clinician. Age, blood counts, cardiovascular risk factors, medical history, and the performing laboratory's reporting criteria all matter.
No clonal signal detected
No reportable mutation is found across the 15-gene scope. This lowers concern from this assay but does not eliminate cardiovascular or blood-cancer risk.
Clonal signal detected
One or more acquired mutations are reported with the laboratory's available clone context. A detected clone is not a diagnosis. Its meaning depends on the gene, clone features, blood counts, history, and standard risk assessment.
How much the Lucence CardioHemeRISK costs
Compare exact Mito member and non-member prices with recently checked comparable offers. Collection and lab fees are shown separately.
| Lab | Test price | Collection or lab fee |
|---|---|---|
| Mito member | $642.60 | $0.00 Added once per order |
| Mito non-member | $899.64 | $0.00 Added once per order |
Mito prices come from the live catalog for the selected provider.
How it works
What to expect from your Lucence CardioHemeRISK
- 1 Book instantly
Click, book, done. Choose a convenient lab location near you. Transparent, up-front pricing.
- 2 Quick lab visit
Testing to fit your schedule, usually 15 minutes or less. Walk-in and appointments available. No fasting needed.
- 3 Results in about 12 working days
Your result posts straight to your dashboard as soon as the lab completes it.
- 4 Expert guidance
With membership, a clinician reviews your result and a personalized action plan follows, with clear next steps.
Every result comes with a plan
A number on its own does not tell you much. Membership is what turns it into next steps, and keeps track of what changes.
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Insights that connect the dots. A clinician reads your whole picture, not one result in isolation, connecting family history, past results, and lifestyle into clear next steps.
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Your personalized action plan. Nutrition, supplements, and training in one clinician-reviewed protocol, updated as your results change.
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Track your trends. Upload results from any lab and see each biomarker trend over time, so you know what is working.
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Never miss a recheck. Mito tells you what is worth retesting and when, then reminds you so nothing slips.
Lucence CardioHemeRISK testing you can trust
Run to clinical-grade standards
- Processed at the same CLIA and CAP-accredited national labs your doctor uses
- Order online, no doctor visit or referral needed
- Your data is encrypted, handled under HIPAA, and never sold
Overseen by our Care Team Lead
Every result, including your Mito Brain analysis, is checked by Rhonda Collins, FNP-C, our Care Team Lead and a board-certified Family Nurse Practitioner with over 15 years of nursing experience across cardiac ICU, primary care, and dermatology.
Meet RhondaWhat members are saying
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@nasdaily
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15/10 experience - I felt actually taken care of
Super impressed with my Mito experience - the thoroughness of the intake, the data tracking and the doctor's visit.
RS Reena Sudan -
@ellarosemcfadin
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Helped show an overall picture
I would highly recommend this service to anyone that wants a more in-depth picture of their health and labs. The platform is super user friendly.
BS Bo Sal -
@katelyn_kim
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Specific and actionable advice
It felt like, for the first time, I had real data guiding me to make meaningful changes and I've definitely noticed the difference.
MH Maya Hickey -
@bryce_witmer
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Tired of arguing with my PCP
After extensive research, I decided Mito was the best option. The insights were clear and make sense. Mito gave me peace of mind and a path to follow.
JO Josh -
@alexandradawson
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3x the tests for less money
A great alternative to the basic blood work at your local clinic. Love the report card format. Much better value.
P Page -
@daniklass
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Best $9 a month I spend
The action plan changes every time new results come in. I've actually never had a health company recommend doing less. Refreshing.
DP Devi Patel -
@natalieefer
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Finally, prices that make sense
Every test is published. I can see what it costs and what I save as a member. No surprises.
KT Kenji Tanaka -
@tyler_sarkisian
Everything your health needs,
in one membership
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Every test at our cost
Members pay our cost on every test, with lab fees passed straight through. The full receipt is itemized, never padded.
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Continuous tracking, all in one place
Upload past labs and watch your trends over time. Every marker and visit lives in one longitudinal record, so all your care stays together.
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Year-round clinician support
Text anytime and get clinician-reviewed answers. When you want to go deeper, 1:1 consultations are available at affordable rates.