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Details of Gene

Item Details
Gene/Locus name

MYO7A (also called NSRD2)

Long Name

myosin VIIA (OMIM 276903)

Associated Disorders

OMIM 276900 : Usher syndrome, type 1B
OMIM 601317 : Deafness, autosomal dominant 11
OMIM 600060 : Deafness, autosomal recessive 2

Interpretation / Comment

Laboratory methods do not necessarily identify all of the clinically significant variants in a gene. The failure to identify a variant does not necessarily mean that the gene is normal. Variants in a gene may cause more than one disease, and the identification of a clinically significant variant does not necessarily indicate the specific disease that the patient or relatives may be at risk of developing. Conversely, the disease/s associated with a gene might also be caused by mutations in other genes, and the failure to identify a clinically significant variant in one gene does not necessarily alter the clinical diagnosis or risk for relatives.

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