ClinVar Miner

Submissions for variant NM_001308093.3(GATA4):c.390G>A (p.Ala130=)

dbSNP: rs2130070163
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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 RCV002158188 SCV002429088 likely benign Atrioventricular septal defect 4 2021-10-25 criteria provided, single submitter clinical testing

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