ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.1350-16C>G

gnomAD frequency: 0.02594  dbSNP: rs11651555
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522348 SCV001731877 benign Epidermodysplasia verruciformis 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001676016 SCV001893808 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676016 SCV005253044 benign not provided criteria provided, single submitter not provided

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