Genetic analysis for SDHB gene mutations (full sequencing)
This test checks for changes (mutations) in the SDHB gene, which may be linked to certain inherited cancers or other health conditions.
["Helps identify inherited risks for cancer or related disorders by examining gene mutations."]
Key facts at a glance
- LOINC
- 82530-7
- Short code
- SDHB gene Del+Dup + Full Mut Anl Bld/T
- Synonyms
- SDHB gene Del+Dup + Full Mut Anl Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- Specimen volume
- 3 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
Why This Test Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of certain cancers (such as paraganglioma, pheochromocytoma, or renal cell carcinoma), or if you have symptoms or a diagnosis related to these conditions. It can also be part of genetic counseling for individuals at higher risk.
What to Expect Before the Test
No special preparation is needed for this test. A blood sample will be taken from a vein in your arm. You may feel a brief pinch, but it usually doesn’t cause discomfort. If you’re taking blood thinners, inform your provider beforehand.
What the Results Mean
Results can be normal (no mutations detected) or positive (mutations found). A positive result means you carry a genetic change in the SDHB gene, which may increase your risk for specific cancers or other health issues. Results are discussed with your healthcare provider in the context of your medical history.
Possible Outcomes and Next Steps
If a mutation is found, your provider may recommend additional testing, monitoring, or lifestyle adjustments to manage risk. If no mutation is detected, your risk may be lower, but ongoing medical care is still important.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Mutations in the SDHB gene are associated with inherited conditions like hereditary paraganglioma-pheochromocytoma syndrome (HPP), which can lead to tumors in certain organs. Early detection can help guide preventive measures, such as regular screenings or monitoring for symptoms.
Short name
SDHB Gene Mutation Test
Frequently asked questions
Will this test show all possible mutations?
What if I have a family history of these cancers?
How long will it take to get results?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy