ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4182C>T (p.Ala1394=)

dbSNP: rs565771303
Minimum review status: Collection method:
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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 RCV001521652 SCV001731028 benign not provided 2024-10-17 criteria provided, single submitter clinical testing

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