ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.912+15C>T

gnomAD frequency: 0.00002  dbSNP: rs375658877
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002085469 SCV002373938 benign Atrioventricular septal defect 4 2023-12-22 criteria provided, single submitter clinical testing

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