ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.9848T>A (p.Ile3283Asn)

dbSNP: rs1688456281
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV001256931 SCV001433452 likely pathogenic Conduction disorder of the heart 2019-06-10 criteria provided, single submitter clinical testing

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