ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3599del (p.Gly1200fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005006693 SCV005632246 likely pathogenic Autosomal dominant nonsyndromic hearing loss 11; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2024-05-04 criteria provided, single submitter clinical testing

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