ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.2084G>T (p.Gly695Val)

dbSNP: rs63751391
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV002508760 SCV000035598 pathogenic Supranuclear palsy, progressive, 1 2005-09-01 no assertion criteria provided literature only
VIB Department of Molecular Genetics, University of Antwerp RCV000084529 SCV000116665 not provided not provided no assertion provided not provided

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