ClinVar Miner

Submissions for variant NM_000836.4(GRIN2D):c.1551C>T (p.Ile517=)

gnomAD frequency: 0.00817  dbSNP: rs76779682
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000971342 SCV001118984 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000971342 SCV002498492 benign not provided 2024-07-01 criteria provided, single submitter clinical testing GRIN2D: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000971342 SCV005313357 benign not provided criteria provided, single submitter not provided

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