ClinVar Miner

Submissions for variant NM_001134407.3(GRIN2A):c.1306T>C (p.Cys436Arg) (rs1555496111)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV001091975 SCV001248296 pathogenic not provided 2019-01-01 criteria provided, single submitter clinical testing
Bioinformatics Core,Luxembourg Center for Systems Biomedicine RCV000656048 SCV000588324 pathogenic Rolandic epilepsy 2017-01-01 no assertion criteria provided case-control CAADphred>15

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