ClinVar Miner

Submissions for variant NM_001083962.2(TCF4):c.1879+10G>C

dbSNP: rs986184777
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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 RCV001498327 SCV001703077 likely benign Pitt-Hopkins syndrome 2018-12-13 criteria provided, single submitter clinical testing

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