ClinVar Miner

Submissions for variant NM_001386795.1(DTNA):c.1176-12C>T

gnomAD frequency: 0.00001  dbSNP: rs377367164
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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 RCV003108838 SCV003783303 likely benign Left ventricular noncompaction 1 2024-05-15 criteria provided, single submitter clinical testing

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