ClinVar Miner

Submissions for variant NM_002087.4(GRN):c.-8+5G>C (rs63750313)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
VIB Department of Molecular Genetics, University of Antwerp RCV000084418 SCV000116554 not provided not provided no assertion provided not provided
GeneReviews RCV001089936 SCV001245408 pathogenic Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 2020-02-03 no assertion criteria provided literature only

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