ClinVar Miner

Submissions for variant NM_000836.4(GRIN2D):c.87G>A (p.Pro29=)

gnomAD frequency: 0.00007  dbSNP: rs985371816
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001995786 SCV002270220 likely benign not provided 2025-01-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001995786 SCV005194716 uncertain significance not provided criteria provided, single submitter not provided

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