ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.507C>T (p.Asp169=)

gnomAD frequency: 0.00004  dbSNP: rs199720207
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000870757 SCV001012300 benign Intellectual disability, autosomal dominant 8 2024-01-14 criteria provided, single submitter clinical testing
GeneDx RCV001593091 SCV001822833 likely benign not provided 2020-05-04 criteria provided, single submitter clinical testing

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