ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.3150C>T (p.Tyr1050=)

gnomAD frequency: 0.00001  dbSNP: rs371039089
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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 RCV001393914 SCV001595591 likely benign Dilated cardiomyopathy 1JJ 2018-03-24 criteria provided, single submitter clinical testing

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