Hemoglobin Variants by Surface Antibody Screening (Serum/Plasma)
This test checks for different types of hemoglobin in your blood, which may indicate inherited blood disorders like sickle cell disease or other genetic conditions.
["Helps identify rare hemoglobin variants that could affect blood health or require further testing."]
Key facts at a glance
- LOINC
- 42504-1
- Short code
- HBV surface Ab CSF Ql
- Synonyms
- HBV surface Ab CSF Ql
- Category
- chemistry
- Sample
- csf
- Container
- Sterile tube
- Units
- N/A
- Ref low
- 0
- Ref high
- 5
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- CPT
- 82378
- SNOMED
- 394995008
- Specimen volume
- 1-2 mL
- Stability
- Immediate analysis required, Refrigerated: 1h
- Hemolysis max
- 200
- TAT
- 4–24 hours
- Order
- routine
Why This Test Matters
Hemoglobin is the protein in red blood cells that carries oxygen. Some people inherit unusual hemoglobin forms that can cause health problems, such as anemia, pain crises, or organ damage. This test screens for these variants early, allowing for early treatment or genetic counseling if needed.
What to Expect Before the Test
You’ll have a small needle inserted into your arm or hand to draw blood. The process takes about 5 minutes. No special preparation is needed, but tell your doctor if you’re on blood thinners or have a history of bleeding issues.
What the Results Mean
Results show the proportion of different hemoglobin types. Abnormal patterns may signal genetic conditions. Your doctor will discuss findings with you, including next steps like confirmatory testing or genetic counseling.
Common Conditions Linked to This Test
Variants like sickle hemoglobin (HbS) or thalassemia can cause chronic pain, frequent infections, or organ damage. Early detection helps manage symptoms and plan care.
Reference range
Non-smokers: <2.5 ng/mL; Smokers: <5.0 ng/mLN/A
No special preparation required. For PSA, avoid sexual activity for 24-48 hours before the test.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test is used primarily in newborn screening, genetic testing, or diagnosing inherited blood disorders. It helps doctors identify conditions that may require specialized care, such as blood transfusions, pain management, or lifestyle adjustments.
Short name
Hemoglobin Variant Screening
Frequently asked questions
What causes abnormal hemoglobin variants?
How often should I get this test?
Can I prevent hemoglobin variants?
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