ClinVar Miner

Submissions for variant NM_000900.5(MGP):c.62-9del

dbSNP: rs11393307
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000329643 SCV000377158 likely benign Keutel syndrome 2016-06-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001521245 SCV001730552 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV001521245 SCV001756342 likely benign not provided 2019-09-14 criteria provided, single submitter clinical testing

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