ClinVar Miner

Submissions for variant NM_005159.5(ACTC1):c.129+17del

dbSNP: rs730880386
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000157769 SCV000207699 benign Cardiomyopathy 2012-12-27 criteria provided, single submitter clinical testing The variant is found in HCM panel(s).

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