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GTR Home > Laboratories > GeneTech


  • GeneTech
  • ATS GeneTech Private Limited
  • 8-2-293/17/A25, Opposite KBR Park,, Road No. 14, Banjara Hills,
  • Hyderabad, Andhra Pradesh, India 500034
  • Phone: +91 40-23400932
    Fax: +91 40-23407943
    Email: info@genetech.co.in
  • Website: http://www.genetech.co.in/

GTR Lab ID: 269666, Last updated:2020-10-29
Annual Review past due read more


  • Director: Anuradha Udumudi, PhD, Lab Director
    Phone: +91 4023400932
    Fax: +91 4023407943
    Email: anu.udumudi@genetech.co.in
  • Chaitra Lava, PhD, Genetic Counselor
  • Vinata Surabhi, Genetic Counselor

Conditions and tests

  • Achondroplasia1 test
  • alpha Thalassemia1 test
  • Autosomal recessive nonsyndromic hearing loss 1A1 test
  • Benign scapuloperoneal muscular dystrophy with cardiomyopathy1 test
  • beta Thalassemia2 tests
  • Breast-ovarian cancer, familial, susceptibility to, 11 test
  • Breast-ovarian cancer, familial, susceptibility to, 21 test
  • Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency1 test
  • Cystic fibrosis1 test
  • Epidermolysis bullosa simplex due to plakophilin deficiency1 test
  • Factor X deficiency1 test
  • Fragile X syndrome1 test
  • G6PD deficiency1 test
  • Hidrotic ectodermal dysplasia syndrome1 test
  • Holt-Oram syndrome1 test
  • Huntington disease1 test
  • Meckel syndrome, type 11 test
  • Meckel syndrome, type 31 test
  • Meckel syndrome, type 41 test
  • Meckel syndrome, type 61 test
  • Methylmalonic acidemia1 test
  • Multiple endocrine neoplasia, type 11 test
  • Myotonic dystrophy1 test
  • Niemann-Pick disease, type A1 test
  • Niemann-Pick disease, type B1 test
  • Oculocutaneous albinism type 11 test
  • Pyruvate dehydrogenase E1-beta deficiency1 test
  • Pyruvate dehydrogenase E2 deficiency1 test
  • Qualitative or quantitative defects of dystrophin1 test
  • Renal hypodysplasia/aplasia 22 tests
  • Seckel syndrome 11 test
  • Sickle cell-beta-thalassemia1 test
  • Skeletal dysplasia1 test
  • Spermatogenic failure, Y-linked, 21 test
  • Spinal muscular atrophy2 tests
  • Spinocerebellar ataxia type 21 test
  • Tay-Sachs disease1 test
  • Thanatophoric dysplasia type 11 test
  • Thrombophilia due to activated protein C resistance1 test
  • Thrombophilia due to thrombin defect1 test
  • Ullrich congenital muscular dystrophy 11 test
  • Wilson disease1 test

List of services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Prenatal testing
  • Custom Sequence Analysis
  • Carrier testing
  • DNA Banking
  • Genetic counseling
  • Maternal cell contamination study (MCC)
  • Mutation Confirmation
  • Clinical Exome Sequencing
  • Microarray Testing
  • Multiple gene testing using Next Generation Sequencing

List of certifications/licenses


  • National Accreditation Board for Testing and Calibration Laborat, Number: MC-3089, Expiration date: 2021-12-20

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.