ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4788G>A (p.Pro1596=)

gnomAD frequency: 0.00001  dbSNP: rs940051903
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001338200 SCV001531852 likely benign not provided 2024-12-12 criteria provided, single submitter clinical testing

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