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Hemoglobin F (HbF) Variant Test, Qualitative

Published: August 9, 2026Updated: August 16, 2026

This qualitative laboratory test looks for the presence of a specified hemoglobin F variant. It reports whether the targeted variant was detected rather than measuring the amount of HbF.

Quick summary

["A detected result may help explain unusual hemoglobin findings or guide counseling about a possible inherited blood condition."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
28006-5
Short code
Hgb F Vom Ql
Synonyms
Hgb F Vom Ql
Category
hematology
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Ref low
12
Ref high
17.5
Critical range
7 N/A – 20 N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
CPT
85018
SNOMED
900000000000003004
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

What This Test Looks For

Hemoglobin F is normally present in red blood cells, particularly in newborns and during pregnancy. This test checks for a particular genetic change that may alter the structure or production of hemoglobin.

How the Result Is Reported

A “detected” or positive result means the targeted variant was found. A “not detected” result means that the specific variant tested for was not found; it does not exclude every possible hemoglobin disorder.

Why the Test May Be Ordered

A clinician may order this test after unexpected hemoglobin test results, family studies, or evaluation of an inherited anemia or hemoglobin disorder. The results are most helpful when reviewed alongside other laboratory and family information.

Important Limitations

This test examines only the variant or variants included by the laboratory. It may not detect other hemoglobin conditions, deletions, or genetic changes, and results should be interpreted by a qualified healthcare professional.

Reference range

Adult males: 13.5-17.5 g/dL; Females: 12.0-16.0 g/dLN/A

Specimen: serum

No special preparation usually required. Stay well hydrated. Inform your healthcare provider of all medications and supplements you are taking.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Short name

HbF variant analysis

Frequently asked questions

What does a “detected” result mean?
It means the specific HbF variant targeted by the test was found in the sample. A clinician should explain what that finding means for the patient and family members.
Does a “not detected” result rule out a hemoglobin disorder?
No. It means only that the particular variant tested for was not found. Other hemoglobin variants or conditions may still be present and may require additional testing.
No. This is a qualitative variant test. It looks for the presence of a targeted HbF genetic change rather than measuring total HbF or separating all hemoglobin types.
No. This is a qualitative variant test. It looks for the presence of a targeted HbF genetic change rather than measuring total HbF or separating all hemoglobin types.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

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