ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3633C>T (p.Tyr1211=)

gnomAD frequency: 0.00001  dbSNP: rs762101560
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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 RCV001486886 SCV001691367 likely benign not provided 2024-11-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578769 SCV001806073 uncertain significance Autosomal dominant nonsyndromic hearing loss 11 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578770 SCV001806074 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578771 SCV001806075 uncertain significance Usher syndrome type 1 2021-07-14 criteria provided, single submitter clinical testing

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