ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1281-5G>T

dbSNP: rs1280409009
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000642329 SCV000763998 likely benign Arrhythmogenic right ventricular dysplasia 10 2017-12-26 criteria provided, single submitter clinical testing

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