ClinVar Miner

Submissions for variant NM_012216.4(MID2):c.1074-4del

dbSNP: rs758037994
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000513751 SCV000609863 likely benign not provided 2017-04-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000513751 SCV001029199 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001821437 SCV002066078 benign not specified 2019-09-24 criteria provided, single submitter clinical testing

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