ClinVar Miner

Submissions for variant NM_000836.4(GRIN2D):c.3363G>C (p.Leu1121=)

gnomAD frequency: 0.00005  dbSNP: rs769768919
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 RCV000891419 SCV001035237 benign not provided 2025-02-02 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000891419 SCV005313362 benign not provided criteria provided, single submitter not provided

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