ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.2283-20C>T

gnomAD frequency: 0.00068  dbSNP: rs371838579
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513580 SCV001721222 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506602 SCV002807055 likely benign Autosomal dominant nonsyndromic hearing loss 11; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 2022-05-20 criteria provided, single submitter clinical testing

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