ClinVar Miner

Submissions for variant NM_000829.4(GRIA4):c.436C>T (p.Leu146=)

gnomAD frequency: 0.00663  dbSNP: rs2229878
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000963098 SCV001110231 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000963098 SCV002497164 benign not provided 2024-08-01 criteria provided, single submitter clinical testing GRIA4: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000963098 SCV005233409 benign not provided criteria provided, single submitter not provided

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