ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.186G>A (p.Ala62=)

dbSNP: rs1466381420
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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 RCV000542473 SCV000652003 likely benign Atrioventricular septal defect 4 2017-03-19 criteria provided, single submitter clinical testing

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