ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.988-4G>A

dbSNP: rs62079073
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000630770 SCV000751737 likely benign Epidermodysplasia verruciformis 2023-12-27 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528524 SCV001740386 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702532 SCV001929043 benign not specified no assertion criteria provided clinical testing

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