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SCN1B Gene Familial atrial fibrillation type 13 Genetic Test

4,400 د.إ

-21%

The “SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the SCN1B gene, which have been associated with Familial Atrial Fibrillation Type 13. Atrial fibrillation (AF) is a common cardiac rhythm disorder that leads to an irregular and often rapid heart rate. The familial form of this condition suggests a genetic component, where specific gene mutations, such as those in the SCN1B gene, are inherited and can significantly increase the risk of developing AF.

This genetic test plays a crucial role in early detection and management of the condition, particularly for individuals with a family history of atrial fibrillation. By analyzing the DNA for specific mutations in the SCN1B gene, healthcare providers can identify individuals at risk, enabling proactive monitoring and implementation of preventive strategies to mitigate complications associated with atrial fibrillation, such as stroke and heart failure.

The test is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic variants associated with this condition. Given the potential health implications and the benefits of early intervention, the test represents a valuable tool for at-risk individuals and their healthcare teams in managing and potentially preventing the onset of familial atrial fibrillation.

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SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test

At DNA Labs UAE, we offer the SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test to help diagnose and manage familial atrial fibrillation type 13. This genetic test analyzes the SCN1B gene using NGS technology, allowing for the analysis of multiple genes simultaneously.

Test Components and Price

The test is priced at 4400.0 AED and requires a blood sample, extracted DNA, or one drop of blood on an FTA card.

Report Delivery

Once the sample is received, the report will be delivered within 3 to 4 weeks.

Method and Test Type

The SCN1B Gene Familial Atrial Fibrillation Type 13 Genetic Test utilizes NGS technology, which enables comprehensive analysis of the SCN1B gene. This test falls under the category of Cardiovascular Pneumology Disorders.

Referring Doctor and Test Department

This test is recommended by cardiologists and is conducted in our Genetics department.

Pre Test Information

Prior to the test, it is essential to provide the clinical history of the patient undergoing the SCN1B Gene Familial Atrial Fibrillation Type 13 NGS Genetic DNA Test. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by SCN1B Gene Familial Atrial Fibrillation Type 13 NGS Genetic DNA Test gene SCN1B.

Test Details

The SCN1B gene is associated with familial atrial fibrillation type 13, a genetic form of atrial fibrillation. NGS genetic testing can identify any mutations or variations in the SCN1B gene that may contribute to the development of this condition. This test provides valuable information for both diagnosis and management of familial atrial fibrillation type 13.

Test Name SCN1B Gene Familial atrial fibrillation type 13 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Cardiovascular Pneumology Disorders
Doctor Cardiologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for SCN1B Gene Familial atrial fibrillation type 13 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SCN1B Gene Familial atrial fibrillation type 13 NGS Genetic DNA Test gene SCN1B
Test Details

The SCN1B gene is associated with familial atrial fibrillation type 13, which is a type of atrial fibrillation that has a genetic basis. NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that allows for the analysis of multiple genes simultaneously. In the case of familial atrial fibrillation type 13, NGS genetic testing can be used to identify any mutations or variations in the SCN1B gene that may be contributing to the development of the condition. This type of testing can provide valuable information for both diagnosis and management of familial atrial fibrillation type 13.