ClinVar Miner

Submissions for variant NM_002476.2(MYL4):c.164-18T>C

gnomAD frequency: 0.01661  dbSNP: rs115582063
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001534764 SCV001751717 benign not provided 2018-10-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002071922 SCV002350260 benign Atrial fibrillation, familial, 18 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001534764 SCV005249317 benign not provided criteria provided, single submitter not provided

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