Welcome to the Department of Clinical Genetics and Precision Medicine at KIMSHEALTH. We provide comprehensive, personalized genetic services designed to optimize healthcare at every stage of life. By combining state of the art genomic diagnostics with patient centered clinical expertise, our team delivers targeted insights to guide disease prevention, accurate diagnosis and individualized treatment plans.

Powered by our inhouse KIMSHEALTH Genomic Lab (KGL), our multidisciplinary model unites clinicians, molecular scientists, bioinformaticians, cytogeneticists and genetic counselors within a single, collaborative framework enabling seamless interpretation of complex genetic data. We are dedicated to empowering physicians with accurate, actionable and clinically relevant genomic intelligence that directly optimizes patient outcomes.

Key features

Integrated Genetic Consulting and Counseling Pre and post test counseling is seamlessly integrated into the diagnostic journey. Clinical Geneticists and BGC certified Genetic Counselors support patients and families with result interpretation, risk assessment, informed decision making and family management.

Clinician Supported Continuum of Care From initial test selection to final clinical management, our Medical Geneticists support referring physicians at every step of the diagnostic journey delivering clinical expertise, expert peer consultation and comprehensive medical oversight.

Clinician Led Variant Interpretation Complex genomic data are carefully curated and co interpreted by Medical Geneticists and Molecular Scientists, ensuring that every finding is evaluated in the context of the patient’s clinical phenotype and family history.

Clinically Actionable Reporting Reports are structured to deliver diagnostic clarity, refine prognostic assessment and identify relevant therapeutic options. Each report undergoes multidisciplinary review by Clinical Geneticists, PhD Scientists, Bioinformaticians and Genetic Counselors.

Flexible & Precision Driven Diagnostic Strategies We offer tailored testing pathways from targeted gene panels to Whole Exome/ Genome Sequencing (WES/ WGS) and multi omics integration. Testing strategies can be pursued sequentially or concurrently, guided by the clinical indication and urgency.

Ongoing Genomic Data Reanalysis Unresolved cases undergo periodic bioinformatic re evaluation as genomic databases, variant classifications and gene disease associations continue to evolve creating opportunities for new diagnoses over time, without the need for re sampling.

Tumor Board Synergy Complex genomic findings are seamlessly integrated into multidisciplinary tumor boards bringing together surgical, medical, radiation and molecular oncology specialists to translate insights into coordinated care plans.

Free Hereditary Cancer Risk Assessment No cost initial consultations conducted by specialized oncogenetic counselors to review personal and family cancer histories, evaluate hereditary risk factors and determine whether comprehensive genetic testing is indicated.

KIMSHEALTH GENOMICS LAB (KGL) Advanced Genomic & Molecular Diagnosis

Cytogenetics

• Constitutional Karyotyping
• Karyotyping for Hematological Malignancies
• Fluorescence In Situ Hybridization (FISH)

Molecular genetics

• Next-Generation Sequencing (NGS)
• Multiplex Ligation dependent Probe Amplification (MLPA
• Sanger Sequencing
• Real Time Polymerase Chain Reaction (RT-PCR)
• Other PCR Based Tests

Bioinformatics Unit

• Internal data analysis pipelines
• Internal Variant Database

Biochemical Genetics Unit

• Tandem Mass Spectroscopy
• Flurescence Immunoassay
• Newborn Screening Panels

Over 100+ accredited genetic tests and Customised Panels

Comprehensive genetic testing with panels tailored to individual clinical requirements