ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.2409+11G>A

gnomAD frequency: 0.00001  dbSNP: rs775473006
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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 RCV001325158 SCV001516137 likely benign not provided 2024-02-17 criteria provided, single submitter clinical testing

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