ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.5004G>A (p.Leu1668=)

dbSNP: rs771771110
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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 RCV002083213 SCV002371512 likely benign not provided 2021-07-30 criteria provided, single submitter clinical testing

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