ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.1116+13C>T

dbSNP: rs2147200561
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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 RCV002118640 SCV002448080 likely benign not provided 2022-08-31 criteria provided, single submitter clinical testing

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