ClinVar Miner

Submissions for variant NM_004387.4(NKX2-5):c.335-5dup

dbSNP: rs1316920712
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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 RCV002116072 SCV002405931 benign Atrial septal defect 7 2021-08-31 criteria provided, single submitter clinical testing

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