ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.1665-19C>T

gnomAD frequency: 0.00034  dbSNP: rs199867961
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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 RCV001511834 SCV001719143 benign Epidermodysplasia verruciformis 2024-01-13 criteria provided, single submitter clinical testing

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