ClinVar Miner

Submissions for variant NM_005257.6(GATA6):c.765C>T (p.Ala255=)

dbSNP: rs926270539
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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 RCV000868829 SCV001010205 likely benign Atrioventricular septal defect 5 2024-11-11 criteria provided, single submitter clinical testing

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