ClinVar Miner

Submissions for variant NM_000381.4(MID1):c.661-7dup

dbSNP: rs375668839
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177054 SCV000228870 benign not specified 2014-11-30 criteria provided, single submitter clinical testing
GeneDx RCV001573509 SCV001866038 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573509 SCV001799493 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000177054 SCV001930015 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000177054 SCV001975140 benign not specified no assertion criteria provided clinical testing

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