ClinVar Miner

Submissions for variant NM_001378418.1(TCF20):c.1440T>C (p.Thr480=)

dbSNP: rs17002894
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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 RCV002105894 SCV002402509 likely benign not provided 2023-09-26 criteria provided, single submitter clinical testing

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