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Kir3D P1 Deletion Variant in Blood

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

This test checks for a specific genetic variation in your blood that involves a deletion in the KIR3D P1 gene, which plays a role in immune function.

Quick summary

["Understanding your genetic variation may help inform your healthcare provider about potential immune-related considerations."]

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

Key facts at a glance

LOINC
64432-8
Short code
KIR3DP1 del variant Bld/T Ql
Synonyms
KIR3DP1 del variant Bld/T Ql
Category
chemistry
Sample
whole-blood
Container
Lavender-top (EDTA)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Method
molgen
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 healthcare provider may recommend this test if you have a family history of immune disorders, certain blood-related conditions, or if you are considering pregnancy and there is a concern about genetic factors affecting immune compatibility.

What to Expect Before the Test

No special preparation is typically needed. You will provide a blood sample, similar to other routine blood tests. This is a simple, painless procedure.

What the Results Mean

The test identifies whether you carry the KIR3D P1 deletion variant. This genetic variation can influence how your immune system interacts with certain cells, which may be relevant in specific medical contexts such as pregnancy or immune-related treatments.

Common Uses and Considerations

This test is often used in the context of prenatal care to assess immune compatibility between parents or in evaluating immune responses in patients with certain genetic predispositions.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Genetic variations like this deletion can affect how your immune system recognizes and responds to cells from another individual, such as during pregnancy or in transplant scenarios. While this test does not diagnose a specific condition, it provides important genetic information that may guide medical decisions.

Short name

Kir3D P1 Gene Deletion Test

Frequently asked questions

What does a positive result mean?
A positive result indicates you have the KIR3D P1 deletion variant. This genetic variation can influence immune interactions and may be relevant in specific medical contexts, such as pregnancy or immune-related treatments, but it does not indicate a health problem on its own.
Will this test affect my treatment plan?
Possibly. Depending on your clinical situation, your healthcare provider may use this genetic information to tailor treatments, especially in cases involving immune-related conditions or pregnancy. Always discuss the results with your healthcare provider.
Is there any risk or discomfort associated with this test?
The test involves a simple blood draw, which may cause mild discomfort at the site. There are no known risks associated with this genetic testing procedure itself.
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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