ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.4287+16G>A

gnomAD frequency: 0.00006  dbSNP: rs140156070
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002539687 SCV003473807 likely benign Dilated cardiomyopathy 1JJ 2023-03-19 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699625 SCV001920224 benign not specified no assertion criteria provided clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001726620 SCV001963347 likely benign not provided no assertion criteria provided clinical testing

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