ClinVar Miner

Submissions for variant NM_007327.4(GRIN1):c.1335C>T (p.Gly445=)

gnomAD frequency: 0.00001  dbSNP: rs370360183
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001034389 SCV001197731 benign Intellectual disability, autosomal dominant 8 2022-09-07 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV004546593 SCV005041730 likely benign not provided 2024-04-01 criteria provided, single submitter clinical testing GRIN1: BP4, BP7

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