ClinVar Miner

Submissions for variant NM_001378418.1(TCF20):c.62T>C (p.Val21Ala)

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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 RCV003843561 SCV004643717 benign not provided 2024-04-29 criteria provided, single submitter clinical testing

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