clinical-exome-sequencing

Clinical Exome Sequencing

Focusing on significant genes associated with all known clinical phenotypes.

It is one of the Next generation sequencing based test offered by Genes2Me.Clinical Exome Sequencing Panel identifies the molecular basis of rare genetic disorders in individuals who are either carriers of the disease or manifest symptoms. The panel screens coding regions of genes that have been proven to be of clinical importance.

Test Price: ₹35000.00

clinical-exome-sequencing
Coverage
Coverage

Clinical Exome Sequencing is one of the Next generation sequencing based test.

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The human exome consists of complete coding (Exonic) regions of the genome. It encompasses 1-2% of the whole genome, yet contains approximately 85% of disease causing pathogenic variants.
  • Covers more than 6000+ genes encoding for various diseases.
  • Identifies more than 4000+ rare diseases.
  • Identifies SNVs (single nucleotide variant).
  • Includes Mitochondrial Genome Coverage in the same test.

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How it Works
Order a Kit

Order and receive Saliva Collection Kit
 

Collect Your Sample

Collect the Saliva sample from your mouth

Lab Processing

Expert scientific team for highly accurate results

Get Your Reports

Find full results in your Genes2Me account

Genetic Counseling

Pre & post test counseling with a Genetic Expert

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