ClinVar Miner

Submissions for variant NM_138691.3(TMC1):c.2260+19T>A

dbSNP: rs2490000452
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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 RCV003673240 SCV004393205 likely benign not provided 2023-02-04 criteria provided, single submitter clinical testing

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