ClinVar Miner

Submissions for variant NM_002087.4(GRN):c.26C>A (p.Ala9Asp) (rs63751243)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000017386 SCV000037658 pathogenic Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 2011-04-01 no assertion criteria provided literature only
VIB Department of Molecular Genetics, University of Antwerp RCV000084421 SCV000116557 not provided not provided no assertion provided not provided
GeneReviews RCV000017386 SCV001245407 pathogenic Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 2020-02-03 no assertion criteria provided literature only

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