ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.1019+16C>T

gnomAD frequency: 0.00001  dbSNP: rs920565524
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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 RCV002153953 SCV002461035 likely benign not provided 2024-05-06 criteria provided, single submitter clinical testing

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