ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.2595dup (p.Ala866fs)

dbSNP: rs1598826658
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000996667 SCV001151516 likely pathogenic not provided 2018-11-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004004437 SCV004839536 uncertain significance Arrhythmogenic right ventricular cardiomyopathy 2023-10-30 criteria provided, single submitter clinical testing

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