Genetic analysis of SLC22A18 gene mutation status
This test checks whether you carry a specific mutation in the SLC22A18 gene, which may influence how your body processes certain substances or could be linked to certain health conditions.
["This test helps identify if the mutation is present, which may guide further medical evaluation or treatment planning."]
Key facts at a glance
- LOINC
- 34514-0
- Short code
- SLC22A18 gene Mut Anl Bld/T
- Synonyms
- SLC22A18 gene Mut Anl Bld/T
- 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
What This Test Measures
The SLC22A18 gene mutation test examines the DNA sequence of the SLC22A18 gene. Mutations in this gene can affect how your body transports certain chemicals, including drugs and toxins. This test is often used in genetic counseling or when evaluating conditions related to metabolic or transport-related disorders.
Why It Might Be Ordered
Your healthcare provider may recommend this test if you have a family history of genetic conditions linked to SLC22A18 mutations, if you’re being evaluated for a suspected metabolic disorder, or if you’re considering genetic testing for a specific health concern.
Sample Collection and Process
A small amount of whole blood is typically collected via a simple venipuncture. The blood sample is then sent to a laboratory for genetic analysis to detect the presence of the SLC22A18 mutation.
What the Results Mean
Results can be either positive (mutation detected) or negative (mutation not detected). A positive result indicates the presence of the mutation, which may require further evaluation by a healthcare provider to understand its implications for your health.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Mutations in the SLC22A18 gene can play a role in conditions affecting how the body processes substances, such as certain medications or toxins. Identifying these mutations can help guide personalized medical advice, especially in cases involving genetic predispositions to metabolic or transport-related disorders. Consult your healthcare provider for detailed interpretation of results in the context of your health history.
Short name
SLC22A18 Gene Mutation Test
Frequently asked questions
What does a positive result mean?
What if my test result is negative?
How often should I get this test?
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