ClinVar Miner

Submissions for variant NM_002294.3(LAMP2):c.742-16TCT[2] (rs730880476)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000157956 SCV000207891 benign Danon disease; Cardiomyopathy 2014-04-01 criteria provided, single submitter clinical testing The variant is found in DCM,HCM panel(s).
Invitae RCV000864013 SCV001004754 benign Danon disease 2019-09-01 criteria provided, single submitter clinical testing

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