ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.432G>T (p.Ala144=)

dbSNP: rs1356013644
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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 RCV001427205 SCV001629879 likely benign Atrioventricular septal defect 4 2019-11-22 criteria provided, single submitter clinical testing

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