ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4368C>T (p.Ala1456=)

dbSNP: rs993085132
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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 RCV003856684 SCV004660071 likely benign not provided 2022-11-25 criteria provided, single submitter clinical testing

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