ClinVar Miner

Submissions for variant NM_138691.3(TMC1):c.1029+7G>A

dbSNP: rs1222212369
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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 RCV003851711 SCV004660895 likely benign not provided 2023-11-04 criteria provided, single submitter clinical testing

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