ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.571A>G (p.Thr191Ala)

dbSNP: rs753332007
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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 RCV001516787 SCV001725136 benign Pitt-Hopkins syndrome 2022-08-09 criteria provided, single submitter clinical testing

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