Hemoglobin Variant RNA Detection by Probe-Based Assay (Serum/Plasma)
This test checks for genetic variations in your red blood cells that may affect how hemoglobin (the protein that carries oxygen) functions. Certain variants can cause conditions like sickle cell disease or other hemolytic anemias.
["Detects rare genetic changes in hemoglobin that could impact blood health."]
Key facts at a glance
- LOINC
- 103618-5
- Short code
- HBV RNA # SerPl NAA+probe
- Synonyms
- HBV RNA # SerPl NAA+probe
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
Why This Test Might Be Ordered
Your doctor may recommend this test if you have symptoms like fatigue, pain, frequent infections, or if you have a family history of hemoglobin disorders. It’s also used in prenatal screening or before certain medical procedures to assess red blood cell health.
This test uses a specialized probe to detect specific RNA sequences from hemoglobin variants in your blood sample. The sample is typically taken from serum or plasma, and the results help identify genetic differences that might not be visible through standard blood tests.
The test involves analyzing a small amount of your blood to identify RNA fragments linked to hemoglobin variants. This method is highly sensitive and can detect even subtle genetic changes that might not be apparent in standard hemoglobin tests.
What to Expect Before the Test
There are usually no special preparations needed. You may have a small needle inserted to draw blood from your arm. If you’re pregnant or have a history of bleeding disorders, let your doctor know before the test.
What the Results Mean
If the test finds hemoglobin variants, it may indicate an inherited condition like sickle cell disease or another genetic disorder. Your doctor will discuss the results with you and may recommend further testing or monitoring based on your symptoms and family history.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
Hemoglobin Variant Screening
Frequently asked questions
What does a positive result mean?
How long does it take to get results?
Can I fast before this test?
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