ClinVar Miner

Submissions for variant NM_004387.4(NKX2-5):c.*296G>C

gnomAD frequency: 0.00009  dbSNP: rs540202205
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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 RCV002216030 SCV002372076 benign Atrial septal defect 7 2023-04-05 criteria provided, single submitter clinical testing

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