ClinVar Miner

Submissions for variant NM_001371986.1(UNC80):c.9509-8A>G

gnomAD frequency: 0.00001  dbSNP: rs1384585896
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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 RCV000935255 SCV001080997 likely benign not provided 2023-06-18 criteria provided, single submitter clinical testing

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