ClinVar Miner

Submissions for variant NM_005257.6(GATA6):c.1428+9T>A

dbSNP: rs751665524
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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 RCV001501563 SCV001706377 likely benign Atrioventricular septal defect 5 2019-10-15 criteria provided, single submitter clinical testing

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