ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4326C>G (p.Pro1442=)

dbSNP: rs76633938
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001500803 SCV001705603 likely benign not provided 2025-01-26 criteria provided, single submitter clinical testing

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