ClinVar Miner

Submissions for variant NM_000301.5(PLG):c.2302G>A (p.Glu768Lys)

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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 RCV002948496 SCV003274699 likely benign not provided 2025-01-01 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV002948496 SCV003811180 uncertain significance not provided 2021-12-08 criteria provided, single submitter clinical testing

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