ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.1546+6T>C

gnomAD frequency: 0.00052  dbSNP: rs199999513
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000343655 SCV000332523 uncertain significance not provided 2015-07-09 criteria provided, single submitter clinical testing
GeneDx RCV000343655 SCV001780469 likely benign not provided 2020-09-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000343655 SCV002459736 likely benign not provided 2022-06-04 criteria provided, single submitter clinical testing

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