ClinVar Miner

Submissions for variant NM_053274.3(GLMN):c.40-6del

dbSNP: rs372630078
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001605 SCV001159028 benign Glomuvenous malformation 2023-11-29 criteria provided, single submitter clinical testing
GeneDx RCV001572980 SCV001910199 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001572980 SCV001798189 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001700966 SCV001918898 benign not specified no assertion criteria provided clinical testing

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