ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.*4423AATT[1]

dbSNP: rs10547766
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000285646 SCV000465542 likely benign Nonsyndromic Hearing Loss, Recessive 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000342931 SCV000465543 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001613188 SCV001839961 benign not provided 2021-05-21 criteria provided, single submitter clinical testing

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