ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4665G>A (p.Pro1555=)

gnomAD frequency: 0.00004  dbSNP: rs371917612
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 RCV001488264 SCV001692772 likely benign not provided 2024-10-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001488264 SCV005206637 likely benign not provided criteria provided, single submitter not provided

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