ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1198-7C>T

gnomAD frequency: 0.00006  dbSNP: rs202163066
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000427214 SCV000533962 likely benign not provided 2021-05-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001522763 SCV001732362 benign Intellectual disability, autosomal dominant 8 2024-01-29 criteria provided, single submitter clinical testing

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