ClinVar Miner

Submissions for variant NM_005257.6(GATA6):c.948G>A (p.Ala316=)

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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 RCV005079665 SCV005725192 likely benign Atrioventricular septal defect 5 2024-02-29 criteria provided, single submitter clinical testing

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