ClinVar Miner

Submissions for variant NM_001696.4(ATP6V1E1):c.531-14dup

dbSNP: rs35683311
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001557916 SCV001779765 likely benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001557916 SCV002446034 benign not provided 2025-01-30 criteria provided, single submitter clinical testing

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