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Nx Gen Sequencing: Dementia Test

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Nx Gen Sequencing: Dementia Test

Short Name: Nx Gen Dementia Test

Nx Gen Sequencing: Dementia Test test available at DNA Labs India for ₹23,400. Uses NGS, Sanger sequencing on Whole blood samples. Results in 40 Working days. Free home collection in 300+ cities across India.

Neurological Genetic TestAdults🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of Nx Gen Sequencing for dementia is to identify genetic mutations that may contribute to the development of dementia. By analyzing genes like APOE, APP, MAPT, and PSEN1, this test aids in diagnosis, prognosis, and the creation of personalized treatment plans. It helps healthcare providers tailor therapies to individual genetic profiles, potentially improving management and slowing disease progression.

Test Code
1333
Price
₹23,400
Sample Type
Whole blood
Result Time
40 Working days
Fasting Required
No
Method
NGS, Sanger sequencing
Step 1

Sample Collection

Duly filled Whole Exome Sequencing Consent Form (Form 37) is mandatory. No fasting required.

Method: Venipuncture

Step 2

Laboratory Analysis

A blood sample is collected via venipuncture into 2 Lavender Top (EDTA) tubes.

Step 3

Report Delivery

Sample should be shipped refrigerated and not frozen. Store at room temperature for up to 6 hours or refrigerated for up to 72 hours.

Timeline: 40 Working days

Patient Instructions

1
Before the Test:Complete the mandatory Whole Exome Sequencing Consent Form (Form 37). No fasting is required.
2
During the Test:Blood sample collection takes a few minutes; procedure is similar to a standard blood draw.
3
After the Test:Sample is sent to the lab for analysis. Results are available in 40 working days.

About This Test

Who Should Get This Test

The purpose of Nx Gen Sequencing for dementia is to identify genetic mutations that may contribute to the development of dementia. By analyzing genes like APOE, APP, MAPT, and PSEN1, this test aids in diagnosis, prognosis, and the creation of personalized treatment plans. It helps healthcare providers tailor therapies to individual genetic profiles, potentially improving management and slowing disease progression.

How to Prepare

  • Submit 10 mL (5 mL min.) whole blood from 2 Lavender Top (EDTA) tubes.
  • Ship refrigerated. DO NOT FREEZE.
  • Ensure consent form is completed and attached.

Doctor's Notes

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

"Early genetic testing for dementia can identify underlying causes, enabling personalized treatment plans and better management strategies."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeWhole blood
Sample Volume10 mL (5 mL min.)
Container2 Lavender Top (EDTA) tubes
Collection MethodVenipuncture

Sample Stability

Room Temperature6 hrs
Refrigerator72 hrs
FrozenNA
Sample Rejection Criteria:
  • Hemolyzed or improperly labeled samples.
  • Insufficient sample volume.
  • Missing or incomplete consent form.

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in dementia-related genes. Positive results may suggest genetic predisposition, while negative results do not rule out dementia.
📊

Pathogenic variant detected

Indicates genetic mutation associated with increased dementia risk; consult a geneticist for counseling and management.

📊

No pathogenic variants detected

No known genetic mutations found; but dementia may have other causes; clinical evaluation recommended.

📊

Variant of uncertain significance

Genetic change with unclear clinical impact; further testing and monitoring may be needed.

⚠️ When to Consult a Doctor:

If experiencing symptoms of dementia, especially with a family history of neurological disorders, consult a neurologist or geneticist promptly for evaluation and possible testing.

Limitations

  • Test may not detect all genetic variants associated with dementia.
  • Results require interpretation by a qualified geneticist or neurologist.
  • Genetic testing has psychological implications and may not predict disease onset with certainty.

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or discomfort.
  • Potential psychological impact from genetic results.
  • Results may require further clinical validation.

Frequently Asked Questions

What is Nx Gen Sequencing for dementia?
It is a genetic test that analyzes DNA to identify mutations in genes associated with dementia, helping in diagnosis and personalized treatment.
How is the test performed?
A blood sample is collected and analyzed using next-generation sequencing (NGS) and Sanger sequencing for accurate genetic profiling.
What genes are tested in this panel?
Genes tested include APOE, APP, CHMP2B, CSF1R, FUS, GRN, MAPT, PRNP, PSEN1, PSEN2, SORL1, TARDBP, TREM2, UBE3A, and VCP.
Is the test painful?
The test involves a standard blood draw, which may cause minor discomfort but is generally not painful.
How accurate is Nx Gen Sequencing?
The test uses advanced sequencing methods for high accuracy, but results should be interpreted by a healthcare professional in clinical context.
What do the results mean?
Results indicate whether pathogenic genetic variants are detected. Positive results suggest genetic risk; negative results do not rule out dementia entirely.
Is this test covered by insurance?
Coverage varies by insurer and policy. It is not typically covered under government schemes like PMJAY; check with your provider.
How should I prepare for the test?
Complete the mandatory consent form (Form 37) and ensure proper sample collection. No fasting is required.
What is the cost of the test?
The test costs INR 23,400, which includes home sample collection for online bookings across India.
Is home sample collection available?
Yes, free home sample collection is available for online bookings in numerous cities across India.
How long does it take to get results?
Results are typically available in 40 working days after sample receipt.
Who should take this test?
Individuals with symptoms of dementia, a family history of neurological disorders, or those seeking genetic insights for personalized healthcare.
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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