ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.655+11G>A

gnomAD frequency: 0.00003  dbSNP: rs755601446
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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 RCV002205723 SCV002366693 likely benign Pitt-Hopkins syndrome 2023-12-11 criteria provided, single submitter clinical testing

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