ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.924C>T (p.Leu308=)

gnomAD frequency: 0.00004  dbSNP: rs370667210
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522603 SCV001732178 benign Epidermodysplasia verruciformis 2023-02-17 criteria provided, single submitter clinical testing

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