ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.779A>C (p.Glu260Ala)

dbSNP: rs782636303
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mayo Clinic Laboratories, Mayo Clinic RCV000660470 SCV000782565 uncertain significance Autosomal dominant nonsyndromic hearing loss 11 2017-01-12 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278608 SCV001465636 uncertain significance Usher syndrome type 1B 2020-04-16 no assertion criteria provided clinical testing

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