ClinVar Miner

Submissions for variant NM_024640.4(YRDC):c.739G>A (p.Gly247Arg)

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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 RCV002834598 SCV003215278 likely benign not provided 2024-02-17 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002834598 SCV004127787 uncertain significance not provided 2023-05-01 criteria provided, single submitter clinical testing

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