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Protein C Gene Mutation Screening (Qualitative)

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

This test checks for genetic variations in the Protein C gene, which may increase your risk of blood clots.

Quick summary

["Genetic screening helps identify potential inherited blood clotting disorders."]

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

Key facts at a glance

LOINC
50682-4
Short code
PRKCG gene CAG Rpt Bld/T Ql
Synonyms
PRKCG gene CAG Rpt Bld/T Ql
Category
chemistry
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Ref low
0.8
Ref high
1.2
Critical range
— – 5 N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
molgen
CPT
85610
SNOMED
396252006
Specimen volume
3 mL
Stability
Room temperature: 4h, Refrigerated: 24h
Hemolysis max
0
Lipemia max
0
Icterus max
0
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 blood clots, recurrent venous thromboembolism (blood clots in veins), or unexplained clotting issues. It may also be part of a broader evaluation for inherited thrombophilia.

What to Expect Before the Test

No special preparation is needed. You’ll provide a blood sample, typically drawn from your arm. The test is usually done in a lab setting and results may take several days to weeks depending on the lab.

What the Test Results Mean

Positive results indicate the presence of specific mutations in the Protein C gene that could raise your risk of clotting. Negative results mean no obvious mutations were found in this test. Discuss results with your healthcare provider to understand your personalized risk and next steps.

Common Conditions Linked to This Test

Protein C deficiency or mutations are associated with an increased risk of blood clots, especially in veins (deep vein thrombosis) or arteries (pulmonary embolism). It’s important to manage risk factors like staying active, avoiding long periods of inactivity, and following any prescribed treatments.

Reference range

INR: 0.8-1.2 (warfarin: 2.0-3.0)N/A

Specimen: whole-blood

Inform your healthcare provider if you are taking blood thinners. No special preparation required.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Short name

Protein C Gene Test

Frequently asked questions

What does a positive result mean for my health?
A positive result suggests you may have a genetic predisposition to blood clots. Your doctor will work with you to assess your risk and recommend personalized strategies, such as blood thinners, lifestyle changes, or monitoring.
How often will I need this test?
The frequency depends on your risk factors and doctor’s recommendations. Some people with a family history may need periodic testing or monitoring, while others may only need it once.
Can I take anything to lower my risk of clots before or after this test?
While this test itself doesn’t affect clot risk, you can reduce risk by staying active, avoiding smoking, managing weight, and following any medication advice from your doctor—even if you’re not taking anticoagulants.
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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