ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.141C>T (p.Arg47=)

dbSNP: rs201039625
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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 RCV001445328 SCV001648356 likely benign Epidermodysplasia verruciformis 2024-01-02 criteria provided, single submitter clinical testing

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