ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.5031G>C (p.Val1677=)

dbSNP: rs1193662289
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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 RCV003859360 SCV004658921 likely benign not provided 2023-06-04 criteria provided, single submitter clinical testing

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