MYO16 Gene Autism Spectrum, MYO16 Related NGS Genetic Test
Short Name: MYO16 Gene Autism Spectrum NGS Test
Also known as: MYO16 Gene Autism Spectrum Disorder NGS Test, MYO16-Related ASD Genetic Test, Autism Spectrum MYO16 Gene Sequencing Test
MYO16 Gene Autism Spectrum, MYO16 Related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One Drop Blood on FTA Card samples. Results in 3 to 4 weeks after the sample is received by the laboratory.. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
This test is intended to identify mutations in the MYO16 gene that may contribute to autism spectrum disorder. It may support a clinical diagnosis of ASD, assist in genetic counselling, and help family members understand the potential hereditary nature of a MYO16 variant.
- Test Code
- 3903
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One Drop Blood on FTA Card
- Result Time
- 3 to 4 weeks after the sample is received by the laboratory.
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No fasting is required. A pre-test genetic counselling session is recommended to review clinical history and create a family pedigree chart.
Method: Venipuncture / FTA card blood spot
Laboratory Analysis
A small blood sample will be drawn by a trained phlebotomist, or one drop of blood may be placed on an FTA card if that collection method is used.
Report Delivery
You can resume normal activities immediately. The sample will be transported to the laboratory for NGS analysis.
Timeline: 3 to 4 weeks after the sample is received by the laboratory.
Patient Instructions
About This Test
Who Should Get This Test
This test is intended to identify mutations in the MYO16 gene that may contribute to autism spectrum disorder. It may support a clinical diagnosis of ASD, assist in genetic counselling, and help family members understand the potential hereditary nature of a MYO16 variant.
How to Prepare
- Provide the clinical history of the patient, including developmental milestones and behavioural features
- A genetic counselling session to draw a family pedigree is recommended before sample collection
- Blood samples should be collected in the appropriate blood collection tube
- If using an FTA card, ensure one drop of blood is applied and dried before packaging
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"A MYO16 NGS test result should be interpreted in the context of the patient's clinical presentation, family history, and neurological assessment. Genetic counselling is essential, especially if a pathogenic variant or a variant of uncertain significance is identified."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Unlabelled or mislabelled samples
- Clotted blood sample when extracted DNA is required
- Insufficient sample quantity
- Wet or improperly packaged FTA card
Understanding Your Results
Positive / Pathogenic variant detected
Negative / No pathogenic variant detected
Variant of uncertain significance (VUS)
Benign / Likely benign variant
Consult your referring neurologist, developmental specialist, or clinical geneticist after receiving the report, especially if a pathogenic variant or a variant of uncertain significance is detected.
Limitations
- ⚠This is a targeted test for the MYO16 gene only; other autism-related genes are not covered
- ⚠It may not detect all types of genetic changes, such as large deletions or duplications, depending on the assay design
- ⚠A negative or variant of uncertain significance result does not exclude MYO16-related autism disorder
- ⚠The result should not be used alone as a diagnostic criterion for ASD
Risks & Considerations
- ●Minimal risk of pain, bruising, or bleeding at the blood collection site
- ●No significant physical risks with FTA card collection
- ●Potential psychological or emotional stress from variant of uncertain significance or pathogenic finding
Interfering Factors
- ●Inaccurate or incomplete family history can affect interpretation
- ●Poor DNA quality or quantity may reduce sequencing success
- ●Variants of uncertain significance may limit clinical actionability
- ●This single-gene test cannot detect other genetic or chromosomal causes of ASD
Compare With Similar Tests
| Test | MYO16 Gene Autism Spectrum, MYO16 Related NGS Genetic Test | MYO16 Gene NGS | Autism Spectrum Disorder NGS Panel | Chromosomal Microarray | Whole Exome Sequencing |
|---|---|---|---|---|---|
| Comparison | MYO16 Gene Autism Spectrum, MYO16 Related NGS Genetic Test | Targeted sequencing of the MYO16 gene only; focused evaluation when MYO16 involvement is suspected. | Tests multiple genes associated with ASD at once; broader than single-gene MYO16 analysis. | Detects large chromosomal gains or losses linked to autism and complements single-gene sequencing. | Analyses most protein-coding genes; can investigate complex or undiagnosed cases but is more comprehensive and often more expensive. |
Frequently Asked Questions
What is the MYO16 gene?
How is MYO16 related to autism spectrum disorder?
What does the MYO16-related NGS genetic test do?
Who should consider this test?
What sample is required for the test?
Is fasting required before the MYO16 gene test?
How long will the reports take?
What is the price of the MYO16-related NGS test?
Does DNA Labs India provide raw data files with the report?
Can a negative MYO16 test rule out autism spectrum disorder?
Does the MYO16 NGS test cover other autism-related genes?
When should I consult a doctor after receiving the result?
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