Skip to main content
DNA Labs India

MYLK Gene Aortic aneurysm, familial thoracic type 7 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

MYLK Gene Aortic aneurysm, familial thoracic type 7 NGS Genetic Test

Short Name: MYLK Gene Aortic Aneurysm Test

Also known as: MYLK-related aortic aneurysm, Familial thoracic aortic aneurysm type 7 genetic test

MYLK Gene Aortic aneurysm, familial thoracic type 7 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

To identify pathogenic mutations in the MYLK gene that increase the risk of familial thoracic aortic aneurysm type 7, aiding in early diagnosis, risk assessment, and personalized management strategies.

Test Code
2554
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 Weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

No specific preparation required. Inform the healthcare provider about any medications or medical conditions.

Method: Venipuncture or Cheek swab

Step 2

Laboratory Analysis

A small blood sample is drawn via venipuncture or a cheek swab is taken for DNA collection. The procedure is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site if blood is drawn. Resume normal activities immediately.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling is recommended to understand the implications of testing. Provide detailed family medical history.
2
During the Test:Sample collection is performed by a trained professional. The process involves minimal discomfort.
3
After the Test:Results are delivered in 3-4 weeks. Follow-up with a genetic counselor or specialist is advised for interpretation.

About This Test

Who Should Get This Test

To identify pathogenic mutations in the MYLK gene that increase the risk of familial thoracic aortic aneurysm type 7, aiding in early diagnosis, risk assessment, and personalized management strategies.

How to Prepare

  • Ensure proper identification of the patient
  • Use sterile collection equipment
  • Label samples accurately with patient details

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for MYLK mutations is crucial for families with a history of aortic aneurysms to assess risk and guide preventive measures, especially in reproductive planning."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5-10 ml blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or Cheek swab

Sample Stability

Blood samples: stable for 48 hours at room temperature
DNA extracts: stable for several days if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Contaminated or mislabeled samples

Understanding Your Results

Results indicate the presence or absence of mutations in the MYLK gene. A positive result suggests increased risk for familial thoracic aortic aneurysm type 7, while a negative result indicates no detected pathogenic variants.
📊

Positive for pathogenic variant

High risk for developing aortic aneurysm; recommend clinical monitoring and genetic counseling.

📊

Negative for pathogenic variant

No detected mutations; risk may be lower, but clinical evaluation is still advised if symptoms persist.

📊

Variant of Uncertain Significance (VUS)

Further testing and family studies may be needed for clarification.

⚠️ When to Consult a Doctor:

Consult a doctor immediately if you experience symptoms like chest pain, shortness of breath, or fainting, or if you have a family history of aortic aneurysms and test positive for MYLK mutations.

Limitations

  • ⚠May not detect all possible mutations in the MYLK gene
  • ⚠Does not predict the severity or onset age of the condition
  • ⚠Results should be interpreted in conjunction with clinical and family history

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection
  • ●Psychological impact of genetic results may require counseling

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA quality
  • ●Improper sample storage or handling

Compare With Similar Tests

TestMYLK Gene Aortic aneurysm, familial thoracic type 7 NGS Genetic TestTGFBR1 Gene Aortic Aneurysm TestACTA2 Gene Aortic Aneurysm Test
ComparisonMYLK Gene Aortic aneurysm, familial thoracic type 7 NGS Genetic Test

Frequently Asked Questions

What is the MYLK Gene Aortic Aneurysm Test?
It is an NGS genetic test that identifies mutations in the MYLK gene associated with familial thoracic aortic aneurysm type 7.
Who should consider this test?
Individuals with a family history of aortic aneurysms, symptoms like chest pain, or known genetic predispositions.
How is the test performed?
A blood sample or cheek swab is collected and analyzed using next-generation sequencing technology.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
Is the test painful?
The collection process involves minimal discomfort, similar to a standard blood draw.
What do the results mean?
Results indicate the presence or absence of MYLK mutations, which can inform risk assessment and management.
Can the test predict the severity of the condition?
No, it identifies genetic risk but does not predict severity or onset age.
Is genetic counseling recommended?
Yes, counseling is advised before and after testing to understand implications.
How accurate is the NGS technology?
NGS is highly accurate for detecting genetic mutations, with high sensitivity and specificity.
Are there any risks associated with the test?
Risks are minimal, primarily related to blood draw, such as bruising.
What should I do if I test positive?
Consult a healthcare provider for monitoring, management, and family screening.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

Related Tests

MMC (Maternal Myopathy with Cardiomyopathy) Mutation Detection Test

₹11,500

LPA Gene Coronary artery disease, susceptibility to NGS Genetic Test

₹20,000

ITIH4 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test

₹20,000

PPP1R17 Gene Hypercholesterolemia, susceptibility to NGS Genetic Test

₹20,000

APOA1 Gene Hypoalphalipoproteinemia NGS Genetic Test

₹20,000

GJC2 Gene Lymphedema, hereditary, type IC NGS Genetic Test

₹20,000
For Hospitals & Clinics

Reference Laboratory Services

We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

LIMS Integration

Your Data Privacy

Your medical data is protected under Indian law.

✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

Book Your Test

Enter your details and we'll connect you within 15 minutes.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.