ClinVar Miner

Submissions for variant NM_004572.3(PKP2):c.2349G>A (p.Pro783=) (rs753226330)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Integrated Genetics/Laboratory Corporation of America RCV000589049 SCV000698473 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV000640034 SCV000761622 likely benign Arrhythmogenic right ventricular cardiomyopathy, type 9 2017-12-19 criteria provided, single submitter clinical testing
Color RCV000772490 SCV000905669 likely benign Cardiomyopathy 2018-08-17 criteria provided, single submitter clinical testing

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