ClinVar Miner

Submissions for variant NM_001100913.3(PACS2):c.2692G>A (p.Gly898Arg)

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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 RCV002900509 SCV003252032 benign not provided 2023-12-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002900509 SCV004129286 uncertain significance not provided 2022-05-01 criteria provided, single submitter clinical testing

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