ClinVar Miner

Submissions for variant NM_001276345.2(TNNT2):c.53-12del

dbSNP: rs730881094
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000159267 SCV000209213 benign Cardiomyopathy 2012-04-11 criteria provided, single submitter clinical testing The variant is found in DCM panel(s).

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