ClinVar Miner

Submissions for variant NM_001127198.5(TMC6):c.2022-14G>A

gnomAD frequency: 0.00270  dbSNP: rs188155233
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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 RCV001516379 SCV001724652 benign Epidermodysplasia verruciformis 2024-01-23 criteria provided, single submitter clinical testing

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