ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1864+17C>T

gnomAD frequency: 0.00039  dbSNP: rs199730840
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001696779 SCV000535090 likely benign not provided 2018-04-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002060073 SCV002394777 benign Intellectual disability, autosomal dominant 8 2024-01-18 criteria provided, single submitter clinical testing

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