ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.1669-7del

dbSNP: rs531072297
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000226643 SCV000725392 likely benign not provided 2022-10-25 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Invitae RCV001521661 SCV001731041 benign Dilated cardiomyopathy 1JJ 2021-07-03 criteria provided, single submitter clinical testing

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