ClinVar Miner

Submissions for variant NM_004415.4(DSP):c.5745T>C (p.Arg1915=)

dbSNP: rs2113698631
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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 RCV001459824 SCV001663677 likely benign Arrhythmogenic cardiomyopathy with wooly hair and keratoderma; Arrhythmogenic right ventricular dysplasia 8 2020-03-25 criteria provided, single submitter clinical testing

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