Clinical Exome Sequencing

Focusing on significant genes associated with all known clinical phenotypes.

Clinical Exome Sequencing is one of the Next Generation Sequencing (NGS) based test offered by Genes2Me. In this panel we identify the molecular basis of rare genetic disorders in individuals who are either carriers of the disease or manifest symptoms at a sequencing depth of >100x. The panel screens coding regions of genes that have been proven to be of clinical importance. 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. 
Genes2Me clinical exome sequencing test for known inherited disorders which covers all exons for near about 7K genes associated with various diseases.


Clinical Exome Sequencing Coverage

Neurology Cardiology Ear, Nose, Throat  Nephrology
Endocrinology Gastroenterology Ophthalmology Metabolic Conditions
Reproductive Health Dermatology  Immunology


Test Price: ₹35000.00

Why Genes2Me for Exome Sequencing?
Why Genes2Me for Exome Sequencing?


  • Covers more than 7000+ genes encoding for various diseases
  • Includes Mitochondrial Genome Coverage in the same test.
  • Superior uniformity enables accurate variant calling with minimal sequencing cost and on-target performance with highest level of gene coverage.
  • Provision of result confirmation with Sanger sequencing.
  • Faster TAT (Turn-Around-Times) for the test of 5-6 weeks.
  • Option of Genetic Counseling to customers.

Complete insight into your health today, bridged with the answers for Tomorrow


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