ClinVar Miner

Submissions for variant NM_002473.5(MYH9):c.*1399C>T

gnomAD frequency: 0.00076  dbSNP: rs544966086
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000397127 SCV000483987 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000299539 SCV000483988 likely benign MYH9-related disorder 2016-06-14 criteria provided, single submitter clinical testing

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