ClinVar Miner

Submissions for variant NM_002473.6(MYH9):c.*198dup

dbSNP: rs886057475
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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 RCV000330467 SCV000438278 uncertain significance MYH9-related disorder 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000387346 SCV000438279 uncertain significance Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing

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