ClinVar Miner

Submissions for variant NM_001130144.3(LTBP3):c.76CTG[11] (p.Leu35dup)

dbSNP: rs71036212
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000533408 SCV000638184 benign Brachyolmia-amelogenesis imperfecta syndrome 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001703196 SCV001960228 benign not provided 2021-06-09 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529177 SCV001742205 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001703196 SCV001928325 likely benign not provided no assertion criteria provided clinical testing

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