ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.*1521C>G

dbSNP: rs3203358
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001522973 SCV001732615 benign Atrioventricular septal defect 4 2025-01-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713018 SCV005272419 benign not provided criteria provided, single submitter not provided

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