ClinVar Miner

Submissions for variant NM_025150.5(TARS2):c.513-10_513-8del

dbSNP: rs587648372
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001513146 SCV000567021 likely benign not provided 2021-06-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001513146 SCV001720695 benign not provided 2024-01-03 criteria provided, single submitter clinical testing

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