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Hemoglobin S Disease Screening (Qualitative)

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

This test checks for the presence of hemoglobin S, a variant of hemoglobin that can cause sickle cell disease or trait. It helps determine if you may have inherited a gene linked to this condition.

Quick summary

["This screening helps identify if you carry the genetic mutation associated with sickle cell disease or trait."]

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

Key facts at a glance

LOINC
46766-2
Short code
Hemoglobin SC Disease DBS-Imp
Synonyms
Hemoglobin SC Disease DBS-Imp
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

Why This Test Matters

Sickle cell disease is a genetic blood disorder where red blood cells become misshapen and can block blood flow, causing pain, infections, and other complications. Screening is important for early detection, especially if you or your family have a history of sickle cell disease or trait.

How the Test Works

This test uses a simple blood sample to detect hemoglobin S through a qualitative method, often involving electrophoresis or another lab technique that separates different types of hemoglobin.

What to Expect Before the Test

You may have a small needle inserted into your arm to draw a blood sample. The process is quick and usually painless. No special preparation is needed, but inform your doctor if you are pregnant or have bleeding disorders.

What the Results Mean

A positive result means you have hemoglobin S in your blood, which may indicate sickle cell trait or disease. A negative result means you do not have this variant. Consult your healthcare provider for further evaluation if needed.

Reference range

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

Specimen: serum

No special preparation required. Stay well hydrated.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Clinical Significance

Short name

HbS Screening

Frequently asked questions

What does a positive result mean?
A positive result suggests you may carry the gene for sickle cell trait. If both parents have the trait, there’s a 25% chance their child will inherit the disease. If you have symptoms like pain, fatigue, or frequent infections, further testing may be recommended.
What does a negative result mean?
A negative result means you do not have detectable hemoglobin S in your blood. However, genetic testing may still be needed to confirm if you carry the gene without detectable hemoglobin S (silent carrier).
Can I get this test if I’m pregnant?
Yes, this screening is often recommended for pregnant individuals with a family history of sickle cell disease. It helps assess risks to your baby and guides prenatal care decisions.
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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