Genetic test for hemoglobin variant screening (e.g., sickle cell trait/disease)
This blood test checks for specific genetic changes in your hemoglobin, which carry oxygen in your blood. These changes can affect how your blood functions, especially in conditions like sickle cell disease.
["Helps identify inherited blood disorders linked to abnormal hemoglobin."]
Key facts at a glance
- LOINC
- 61165-7
- Short code
- HBV T184I Islt Ql Genotyp
- Synonyms
- HBV T184I Islt Ql Genotyp
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- genotyping
- 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 a family history of hemoglobin disorders, symptoms like fatigue, pain, or frequent infections, or if you’re planning pregnancy and there’s a risk of genetic conditions.
What to Expect Before the Test
You’ll have a small needle inserted into your arm or hand to draw a few drops of blood. It only takes a few minutes, and you may feel a slight pinch. No special preparation is needed, but tell your doctor about any medications you’re taking.
What the Results Mean
Results show whether you carry specific genetic variants in your hemoglobin. For example, a positive test for sickle cell trait means you have one normal and one abnormal hemoglobin gene, which can affect how your blood functions under stress.
Common Conditions Linked to This Test
This test is often used to diagnose or screen for conditions like sickle cell disease, thalassemia, or other hemoglobinopathies. It can also help confirm a diagnosis if symptoms suggest these disorders.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
This test plays a critical role in genetic counseling, prenatal screening, and managing conditions that affect red blood cell health. Early detection can help guide treatment plans and prevent complications.
Short name
Hemoglobin variant genotyping
Frequently asked questions
What does a positive result mean for my health?
How often should I get this test?
Can lifestyle changes help if I have a genetic variant detected?
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