ClinVar Miner

Submissions for variant NM_144498.4(OSBPL2):c.543C>G (p.Pro181=)

dbSNP: rs139386621
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001589856 SCV001823726 likely benign not provided 2020-08-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001589856 SCV002381216 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001589856 SCV005210022 likely benign not provided criteria provided, single submitter not provided

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