ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.-113C>A

gnomAD frequency: 0.00023  dbSNP: rs866593085
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000213904 SCV000271704 uncertain significance not specified 2014-12-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002485383 SCV002779790 uncertain significance Arrhythmogenic right ventricular dysplasia 11 2021-09-06 criteria provided, single submitter clinical testing

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