ClinVar Miner

Submissions for variant NM_000228.3(LAMB3):c.781C>G (p.Pro261Ala)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002962158 SCV003280628 benign not provided 2024-01-17 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002962158 SCV003816413 uncertain significance not provided 2019-05-21 criteria provided, single submitter clinical testing

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