ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.794-11T>A

gnomAD frequency: 0.00002  dbSNP: rs1347697507
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001332981 SCV001525455 uncertain significance Intellectual disability, autosomal dominant 8 2020-02-06 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Labcorp Genetics (formerly Invitae), Labcorp RCV001332981 SCV002327852 likely benign Intellectual disability, autosomal dominant 8 2024-10-31 criteria provided, single submitter clinical testing

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