ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.7093A>G (p.Asn2365Asp)

dbSNP: rs2148728656
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory - Cardiogenetics, CHU de Nantes RCV002260458 SCV002540079 uncertain significance Arrhythmogenic right ventricular cardiomyopathy 2022-06-01 criteria provided, single submitter curation

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