ClinVar Miner

Submissions for variant NM_002335.4(LRP5):c.34CTG[8] (p.Leu20del)

dbSNP: rs72555376
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000173281 SCV000224378 likely benign not specified 2016-08-12 criteria provided, single submitter clinical testing
Invitae RCV001299442 SCV001488529 likely benign not provided 2024-01-16 criteria provided, single submitter clinical testing
GeneDx RCV001299442 SCV001850826 benign not provided 2019-08-19 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001299442 SCV001799494 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001299442 SCV001808249 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000173281 SCV002033922 benign not specified no assertion criteria provided clinical testing

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