ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.1019+19G>A

dbSNP: rs1464645598
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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 RCV003862619 SCV004673355 likely benign not provided 2024-01-02 criteria provided, single submitter clinical testing

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