ClinVar Miner

Submissions for variant NM_001510.4(GRID2):c.1203T>C (p.Leu401=)

gnomAD frequency: 0.00850  dbSNP: rs80091080
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000973238 SCV001120979 benign not provided 2024-01-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000973238 SCV002544881 benign not provided 2024-08-01 criteria provided, single submitter clinical testing GRID2: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000973238 SCV005301345 benign not provided criteria provided, single submitter not provided
Department of Pathology and Laboratory Medicine, Sinai Health System RCV000973238 SCV001550152 uncertain significance not provided no assertion criteria provided clinical testing

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