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Update on Clinical Annotations
If you would like to be updated on the classification of the variant as per the ACMG & AMP guidelines, please access and share the phenotypes after login.
Disclaimer:
This resource is intended for purely research purposes. It should not be used for emergencies or medical or professional advice.
This website does not provide any medical or healthcare products, services or advice, and is
not for medical emergencies or urgent situations. Information contained on this website is not
a substitute for a doctor's medical judgment or advice. We recommend that you discuss your
specific, individual health concerns with your doctor or health care professional.
Commercial use of the resource would require licensing. For more information, contact CSIR-IGIB Business Development and Management Group at s.sivasubbu@igib.res.in
Cite this Resource
Jain A., Bhoyar R.C., Pandhare K., Mishra A., Sharma D., Imran M., Senthivel V., Divakar M.K., Rophina M., Jolly B., Batra A., Sharma S., Siwach S., Jadhao AG., Palande NV., Jha GN., Ashrafi N, Mishra PK, Vidhya A. K., Jain S., Dash D., Kumar NS, Vanlallawma A., Sarma RJ, Chhakchhuak L., Kalyanaraman S., Mahadevan R., Kandasamy S., Pabitha B. M., Rajagopal RE., Ezhil Ramya J., Nirmala Devi P., Bajaj A., Gupta V., Mathew S., Goswami S., Mangla M., Prakash S., Joshi K., Meyakumla, Sreedevi S., Gajjar D.,Soraisham R., Yadav R., Devi YS, Gupta A., Mukerji M., Ramalingam S., Binukumar B. K., Scaria V*, Sivasubbu S* (2020)
IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes.
Nucleic Acids Research, doi: 10.1093/nar/gkaa923. (PMID: 33095885)
https://clingen.igib.res.in/HLA/
