ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.550-20A>T

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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 RCV003507881 SCV004333464 likely benign Pitt-Hopkins syndrome 2023-10-16 criteria provided, single submitter clinical testing

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