ClinVar Miner

Submissions for variant NM_005257.6(GATA6):c.1749C>T (p.Ser583=)

dbSNP: rs142079702
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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 RCV002548304 SCV001112028 likely benign Atrioventricular septal defect 5 2020-05-23 criteria provided, single submitter clinical testing

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