ClinVar Miner

Submissions for variant NM_152468.5(TMC8):c.60G>A (p.Glu20=)

dbSNP: rs1420789594
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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 RCV002183858 SCV002478907 likely benign Epidermodysplasia verruciformis 2021-04-03 criteria provided, single submitter clinical testing

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