Serum/plasma substance concentration (qualitative) for a genetic marker associated with skull morphology or bone density
This test measures a specific genetic component linked to variations in bone structure or skull shape. It may be used in research or specialized clinical contexts to assess inherited traits.
["This test helps identify genetic variations that could influence bone or skull characteristics."]
Key facts at a glance
- LOINC
- 60644-2
- Short code
- Sn-Pg' Skull XR
- Synonyms
- Sn-Pg' Skull XR
- Category
- chemistry
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- xr-measured
- 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 Measures
This test detects the presence or absence of a particular genetic variant related to skull morphology. The result is qualitative, meaning it indicates whether the variant is present or not, without providing a precise quantity.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of unusual bone or skull features, are part of a genetic study, or if specific clinical concerns about bone health or genetic traits are discussed.
How the Test Is Performed
A blood sample is drawn from a vein in your arm. The serum or plasma is then analyzed to check for the genetic marker. The result is typically reported as positive or negative for the variant.
What the Results Mean
A positive result indicates the presence of the genetic variant associated with the measured trait. A negative result means the variant is not detected in this sample. Consult your healthcare provider for interpretation tailored to your specific situation.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance
Short name
Genetic Skull Morphology Marker (Qualitative)
Frequently asked questions
This test may be used in genetic research or specialized clinical settings to understand inherited traits related to bone structure or skull morphology. It could help in diagnosing or monitoring conditions linked to genetic variations in bone health.
The results are qualitative and do not include a numeric range. Your provider will discuss the implications based on your overall health and medical history.
This test may not be covered by all insurance plans, so check with your provider or insurance company before proceeding.
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