ClinVar Miner

Submissions for variant NM_001105206.3(LAMA4):c.2493G>A (p.Lys831=)

dbSNP: rs869025450
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000208045 SCV000263994 uncertain significance Primary dilated cardiomyopathy 2015-10-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494543 SCV002780097 uncertain significance Dilated cardiomyopathy 1JJ 2021-10-29 criteria provided, single submitter clinical testing

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