ClinVar Miner

Submissions for variant NM_002087.3(GRN):c.708+1G>A (rs63749817)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center of Genomic medicine, Geneva,University Hospital of Geneva RCV000503399 SCV000598130 pathogenic Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 2017-02-06 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000513518 SCV000608820 likely pathogenic not provided 2017-02-01 criteria provided, single submitter clinical testing
Institute of Human Genetics,Klinikum rechts der Isar RCV000503399 SCV001150130 pathogenic Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 2019-06-07 criteria provided, single submitter clinical testing
Translational Genetics in Neurodegenerative disease,Karolinska Institutet RCV000185615 SCV000238527 pathogenic Frontotemporal dementia no assertion criteria provided research

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