ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4389C>G (p.Val1463=)

dbSNP: rs2064475705
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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 RCV002148346 SCV002463386 likely benign not provided 2021-11-16 criteria provided, single submitter clinical testing

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