ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.1533+17G>A

gnomAD frequency: 0.00004  dbSNP: rs370228757
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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 RCV002200861 SCV002488812 likely benign Epidermodysplasia verruciformis 2022-03-12 criteria provided, single submitter clinical testing

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