ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.185C>T (p.Thr62Met)

dbSNP: rs782412089
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001578772 SCV001806076 uncertain significance Autosomal dominant nonsyndromic hearing loss 11 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578773 SCV001806077 uncertain significance Autosomal recessive nonsyndromic hearing loss 2 2021-07-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001578774 SCV001806078 uncertain significance Usher syndrome type 1 2021-07-14 criteria provided, single submitter clinical testing

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