ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.1656T>C (p.Asn552=)

gnomAD frequency: 0.00001  dbSNP: rs1217138981
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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 RCV001439785 SCV001642679 likely benign Pitt-Hopkins syndrome 2020-10-09 criteria provided, single submitter clinical testing

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