Multigene Panel Analysis for Blood (Genetic Testing)
This test examines multiple genes in your blood sample to identify potential inherited conditions or variations that may affect health.
["Helps detect genetic factors that could influence disease risk or treatment options."]
Key facts at a glance
- LOINC
- 99971-4
- Short code
- HLH multigene analysis Bld/T
- Synonyms
- HLH multigene analysis Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Ref low
- 1.5
- Ref high
- 9
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- CPT
- 83002
- 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
What This Test Measures
This test analyzes a selection of genes associated with various inherited conditions. It looks for specific DNA changes (mutations, variations, or differences) that may be linked to conditions like metabolic disorders, cancer predispositions, or other genetic syndromes. The test may also assess gene expression patterns or functional impacts of these genetic variations.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of certain genetic conditions, symptoms suggestive of a genetic disorder, or if you’re considering genetic counseling or preconception testing. It can also be used in research or for specific clinical scenarios where multiple genes are relevant.
Sample Collection and Preparation
A blood sample is drawn from your arm, similar to a routine blood test. The sample is processed to extract DNA for genetic analysis. This process is typically done in a laboratory setting and may take several days to complete, depending on the complexity of the panel.
What to Expect Before or After the Test
There are usually no special preparations needed before the test. You may experience mild discomfort from the blood draw, but this is common and temporary. Results may take weeks to months, depending on the testing facility and the complexity of the analysis. Follow-up with your healthcare provider is important to discuss results and next steps.
Reference range
Follicular: 1.5-9.0 mIU/mLN/A
For females: inform if menstrual cycle status. For certain tests, timing within menstrual cycle may matter.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
Genetic Blood Test
Frequently asked questions
Identifying genetic variations can help determine if you’re at higher risk for certain conditions, guide personalized treatment plans, or inform decisions about family planning. Some findings may be actionable (e.g., lifestyle changes, medications), while others may require further evaluation or genetic counseling.
How accurate is this test?
What if my test results are abnormal?
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