ClinVar Miner

Submissions for variant NM_001127198.5(TMC6):c.1228-8G>A

gnomAD frequency: 0.00990  dbSNP: rs150703149
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000554651 SCV000626069 benign Epidermodysplasia verruciformis 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004710083 SCV005254461 benign not provided criteria provided, single submitter not provided

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