ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.5113-15T>C

gnomAD frequency: 0.00001  dbSNP: rs1554322953
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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 RCV002143339 SCV002453398 likely benign Dilated cardiomyopathy 1JJ 2021-09-22 criteria provided, single submitter clinical testing

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