ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.3415-9C>T

gnomAD frequency: 0.00002  dbSNP: rs782551665
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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 RCV001473630 SCV001677784 likely benign Dilated cardiomyopathy 1JJ 2024-11-15 criteria provided, single submitter clinical testing

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