ClinVar Miner

Submissions for variant NM_001145809.2(MYH14):c.1330-17T>C

gnomAD frequency: 0.00346  dbSNP: rs146235441
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001538110 SCV001755718 likely benign not provided 2020-06-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001538110 SCV002373349 benign not provided 2024-01-17 criteria provided, single submitter clinical testing

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