ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.1716C>T (p.Gly572=)

gnomAD frequency: 0.00001  dbSNP: rs1163635070
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502427 SCV000597760 likely benign not specified 2016-01-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001437456 SCV001640309 likely benign not provided 2024-10-30 criteria provided, single submitter clinical testing

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