ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.1296C>T (p.Val432=)

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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 RCV005151169 SCV005776793 likely benign Atrioventricular septal defect 4 2024-08-11 criteria provided, single submitter clinical testing

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