ClinVar Miner

Submissions for variant NM_002335.4(LRP5):c.34CTG[7] (p.Leu19_Leu20del)

dbSNP: rs72555376
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000278068 SCV000340468 uncertain significance not provided 2016-03-31 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000278068 SCV001538112 likely benign not provided 2025-01-27 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, The Hospital for Sick Children RCV002278301 SCV002564925 uncertain significance Osteogenesis imperfecta 2021-10-21 criteria provided, single submitter clinical testing

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