ClinVar Miner

Submissions for variant NM_001510.4(GRID2):c.855G>A (p.Arg285=)

gnomAD frequency: 0.01001  dbSNP: rs75225211
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000971742 SCV001119406 benign not provided 2025-01-20 criteria provided, single submitter clinical testing
GeneDx RCV000971742 SCV002104473 likely benign not provided 2021-05-05 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000971742 SCV004011550 benign not provided 2024-07-01 criteria provided, single submitter clinical testing GRID2: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000971742 SCV005260213 likely benign not provided criteria provided, single submitter not provided

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