ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.1551+8G>A

gnomAD frequency: 0.00006  dbSNP: rs782128294
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000200252 SCV000250524 benign not specified 2014-09-05 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV001523058 SCV001732709 benign Dilated cardiomyopathy 1JJ 2023-10-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001523058 SCV002807167 likely benign Dilated cardiomyopathy 1JJ 2021-10-22 criteria provided, single submitter clinical testing

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