ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4759C>T (p.Leu1587=)

gnomAD frequency: 0.00003  dbSNP: rs749374620
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 RCV001475358 SCV001679548 likely benign not provided 2024-10-15 criteria provided, single submitter clinical testing

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