ClinVar Miner

Submissions for variant NM_000836.4(GRIN2D):c.2031G>A (p.Leu677=)

gnomAD frequency: 0.00001  dbSNP: rs780682575
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002167982 SCV002342614 likely benign not provided 2020-12-30 criteria provided, single submitter clinical testing

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