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ZCCHC12 Gene Mental retardation non-syndromic NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

ZCCHC12 Gene Mental retardation non-syndromic NGS Genetic Test

Short Name: ZCCHC12 Gene Test

Also known as: ZCCHC12 gene NGS test, ZCCHC12 intellectual disability test, Genetic test for non-syndromic mental retardation

ZCCHC12 Gene Mental retardation non-syndromic 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

🩺 Medically Reviewed By

Overview

To identify pathogenic variants in the ZCCHC12 gene that may cause non-syndromic mental retardation, aiding in diagnosis, management, and family planning.

Test Code
1681
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

Provide clinical history of the patient. A genetic counseling session is recommended to draw a pedigree chart of family members affected with similar conditions. No specific preparation is required, but ensure all documentation is ready.

Method: Venipuncture or FTA card collection

Step 2

Laboratory Analysis

Standard blood draw via venipuncture or collection of a blood drop on FTA card. Ensure proper labeling and handling of the sample.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Store samples at ambient room temperature as instructed. Await report in 3-4 weeks.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history review are essential. Ensure informed consent is obtained from the patient or guardian.
2
During the Test:Sample collection is minimally invasive, involving a blood draw. The sample is processed in the lab using NGS technology.
3
After the Test:Report will be available in 3-4 weeks. Follow-up genetic counseling is recommended to discuss results and implications.

About This Test

Who Should Get This Test

To identify pathogenic variants in the ZCCHC12 gene that may cause non-syndromic mental retardation, aiding in diagnosis, management, and family planning.

How to Prepare

  • No fasting required
  • Bring clinical history and genetic counseling notes
  • Use sterile collection tubes or FTA cards
  • Ensure sample is labeled correctly with patient details

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"Genetic testing for the ZCCHC12 gene can help identify underlying genetic causes of intellectual disability, guiding personalized management, family counseling, and early intervention strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Collection MethodVenipuncture or FTA card collection

Sample Stability

Blood samples stable for 24 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Incorrectly labeled or contaminated samples

Understanding Your Results

Results are interpreted based on the presence or absence of pathogenic variants in the ZCCHC12 gene. A positive result indicates a likely genetic cause for non-syndromic mental retardation, while a negative result does not exclude other genetic or environmental factors.
Normal: No pathogenic variants detected – consider other genetic or non-genetic causes
Abnormal: Pathogenic variant identified – confirm with genetic counseling and discuss management
Variant of uncertain significance (VUS) – require further investigation and family studies
⚠️ When to Consult a Doctor:

Consult a geneticist or neurologist if results indicate a pathogenic variant, for personalized management, family risk assessment, and counseling. Also seek consultation if symptoms persist despite negative results.

Limitations

  • May not detect all types of genetic mutations (e.g., large deletions, intronic variants)
  • Results require interpretation by a clinical geneticist
  • Genetic testing cannot predict severity or progression of symptoms

Risks & Considerations

  • Minimal risk from blood draw (e.g., bruising, infection)
  • Psychological impact of test results
  • Potential for uncertain findings requiring further testing

Interfering Factors

  • Poor sample quality or DNA degradation
  • Contamination during sample handling
  • Recent blood transfusion may affect results

Compare With Similar Tests

TestZCCHC12 Gene Mental retardation non-syndromic NGS Genetic TestFMR1 Gene Test for Fragile X SyndromeMECP2 Gene Test for Rett SyndromeWhole Exome Sequencing (WES)Chromosomal Microarray Analysis
ComparisonZCCHC12 Gene Mental retardation non-syndromic NGS Genetic TestTargets a different genetic cause of intellectual disability with specific featuresFocused on a syndromic form of intellectual disability, primarily in femalesBroader analysis of multiple genes, may identify variants in ZCCHC12 and othersDetects chromosomal abnormalities, not specific to ZCCHC12 mutations

Frequently Asked Questions

What is the ZCCHC12 gene test?
It is a genetic test using NGS technology to detect mutations in the ZCCHC12 gene associated with non-syndromic mental retardation or intellectual disability.
Who should consider this test?
Individuals with symptoms of intellectual disability, delayed milestones, or a family history of similar conditions, as recommended by a healthcare provider.
How is the sample collected?
Via blood draw or a blood drop on an FTA card, with free home collection available in many cities across India.
Is fasting required for this test?
No, fasting is not required for the ZCCHC12 gene test.
What is the cost of the test?
The test costs INR 20000, with no hidden charges, and includes sample collection and analysis.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
What do positive results mean?
A positive result indicates a pathogenic variant in the ZCCHC12 gene, suggesting a genetic cause for intellectual disability. Consult a geneticist for interpretation.
Can this test diagnose other conditions?
No, it specifically targets ZCCHC12 gene mutations. For comprehensive analysis, consider broader genetic tests like whole exome sequencing.
Is genetic counseling required?
Yes, genetic counseling is recommended before and after the test to understand implications and guide decision-making.
What if the results are uncertain?
If a variant of uncertain significance (VUS) is found, further testing or family studies may be needed. Consult your genetic counselor.
Is the test available for children?
Yes, the test can be performed on individuals of any age, but consent from a guardian is required for minors.
How accurate is the NGS technology used?
NGS is highly accurate for detecting genetic variants, but no test is 100% conclusive. Results should be interpreted in clinical context.
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.

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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.

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