ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.669-4G>C

dbSNP: rs8079824
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000541088 SCV000626091 benign Epidermodysplasia verruciformis 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001653886 SCV001862458 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001653886 SCV005253033 benign not provided criteria provided, single submitter not provided

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