ClinVar Miner

Submissions for variant NM_014000.3(VCL):c.2454G>A (p.Leu818=)

gnomAD frequency: 0.00001  dbSNP: rs781226887
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002099283 SCV002433375 likely benign Dilated cardiomyopathy 1W 2021-04-10 criteria provided, single submitter clinical testing

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