ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1038G>A (p.Lys346=)

dbSNP: rs1555627111
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000642334 SCV000764003 likely benign Arrhythmogenic right ventricular dysplasia 10 2017-10-13 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003532221 SCV004363178 likely benign Cardiomyopathy 2021-09-07 criteria provided, single submitter clinical testing

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