ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.1823+20C>G

gnomAD frequency: 0.00002  dbSNP: rs780193567
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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 RCV002212807 SCV002361640 benign Epidermodysplasia verruciformis 2023-12-31 criteria provided, single submitter clinical testing

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