ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.2727C>T (p.Ser909=)

dbSNP: rs375889859
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001430994 SCV001633744 likely benign not provided 2024-10-23 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001820125 SCV002064808 likely benign not specified 2020-10-12 criteria provided, single submitter clinical testing

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