ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.1078+19dup

dbSNP: rs144408691
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246807 SCV000310764 benign not specified criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000293454 SCV000465376 likely benign Nonsyndromic Hearing Loss, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000350660 SCV000465377 likely benign Nonsyndromic Hearing Loss, Recessive 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001610655 SCV001832997 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Invitae RCV001610655 SCV002453358 benign not provided 2024-01-31 criteria provided, single submitter clinical testing

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