ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.-543C>T

gnomAD frequency: 0.17297  dbSNP: rs61277615
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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 RCV001520285 SCV001729348 benign Atrioventricular septal defect 4 2023-12-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004713014 SCV005272396 benign not provided criteria provided, single submitter not provided

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