ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.4734C>T (p.Asp1578=)

gnomAD frequency: 0.00001  dbSNP: rs747155741
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001435516 SCV001638340 likely benign not provided 2023-10-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578725 SCV001806017 uncertain significance Autosomal dominant nonsyndromic hearing loss 11 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578726 SCV001806018 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578727 SCV001806019 uncertain significance Usher syndrome type 1 2021-07-14 criteria provided, single submitter clinical testing

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