ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.148G>T (p.Val50Leu)

dbSNP: rs755628496
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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 RCV001034482 SCV001197839 likely benign Pitt-Hopkins syndrome 2019-11-12 criteria provided, single submitter clinical testing

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