Skip to main content
DNA Labs India

SGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic Test

Short Name: SGCD Cardiomyopathy Genetic Test

Also known as: SGCD Gene Mutation Test, Dilated Cardiomyopathy Type 1L Genetic Test, SGCD Cardiomyopathy NGS Test

SGCD Gene Cardiomyopathy, dilated type 1L 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. 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

The purpose of this test is to identify mutations in the SGCD gene that cause dilated cardiomyopathy type 1L, aiding in diagnosis, family screening, and personalized treatment planning.

Test Code
5216
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
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree.

Method: Venipuncture or Finger prick

Step 2

Laboratory Analysis

Blood sample will be collected by a trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Consult with a healthcare provider to discuss the need for testing and provide informed consent.
2
During the Test:The test involves a simple blood draw; no special procedures required.
3
After the Test:Results will be available in 3-4 weeks; follow up with your doctor for interpretation.

About This Test

Who Should Get This Test

The purpose of this test is to identify mutations in the SGCD gene that cause dilated cardiomyopathy type 1L, aiding in diagnosis, family screening, and personalized treatment planning.

How to Prepare

  • Ensure proper identification
  • Use sterile equipment
  • Label samples correctly

Doctor's Notes

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

"This test is crucial for early diagnosis and management of dilated cardiomyopathy, helping to prevent complications like heart failure."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
ContainerEDTA tube or FTA Card
Collection MethodVenipuncture or Finger prick

Sample Stability

Blood samples stable for 48 hours at room temperature
FTA cards stable for longer periods
Sample Rejection Criteria:
  • Hemolyzed samples
  • Insufficient volume
  • Improperly labeled samples

Understanding Your Results

Results indicate the presence or absence of mutations in the SGCD gene associated with dilated cardiomyopathy type 1L.
📊

Pathogenic variant detected

Confirms diagnosis of SGCD-related cardiomyopathy. Genetic counseling recommended.

📊

No pathogenic variant detected

Reduces likelihood of SGCD-related cardiomyopathy, but clinical correlation is advised.

⚠️ When to Consult a Doctor:

If symptoms persist or if there is a family history of cardiomyopathy, consult a cardiologist or genetic counselor.

Limitations

  • ⚠May not detect all types of mutations
  • ⚠Results require clinical correlation
  • ⚠Genetic variants of uncertain significance may be identified

Risks & Considerations

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

Interfering Factors

  • ●Poor sample quality
  • ●Contamination
  • ●Technical errors in sequencing

Compare With Similar Tests

TestSGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic TestTTN Gene Cardiomyopathy TestLMNA Gene Cardiomyopathy Test
ComparisonSGCD Gene Cardiomyopathy, dilated type 1L NGS Genetic Test

Frequently Asked Questions

What is SGCD Gene Cardiomyopathy, Dilated Type 1L?
It is a genetic disorder caused by mutations in the SGCD gene, leading to dilated cardiomyopathy where the heart muscle becomes weakened and enlarged.
What are the symptoms of this condition?
Common symptoms include shortness of breath, fatigue, chest pain, swelling in legs and ankles, rapid heartbeat, and dizziness or fainting.
How is the test performed?
The test uses Next-Generation Sequencing (NGS) to analyze the SGCD gene from a blood sample or extracted DNA.
What is the cost of the test in India?
The cost is approximately INR 20,000, with home sample collection available across India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
Results indicate if pathogenic mutations in the SGCD gene are detected, which can confirm diagnosis and guide treatment.
Is the test covered by insurance?
Coverage depends on the insurance provider; it is not typically covered under government schemes like PMJAY or CGHS.
Can the test be done for children?
Yes, the test can be performed on individuals of all ages, but genetic counseling is recommended for minors.
What is the accuracy of the test?
NGS technology provides high accuracy for detecting genetic mutations, but results should be correlated with clinical findings.
Are there any risks associated with the test?
Risks are minimal, mainly related to blood draw, such as bruising or infection, and potential psychological impact of results.
How can I prepare for the test?
No special preparation is needed; provide clinical history and family pedigree during genetic counseling.
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.