ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.7966-20del

dbSNP: rs752921347
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000182636 SCV000235009 benign not specified 2013-04-08 criteria provided, single submitter clinical testing The variant is found in ARVC panel(s).

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