ClinVar Miner

Submissions for variant NM_016835.4(MAPT):c.1766G>T (p.Gly589Val) (rs63750376)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000015315 SCV000035574 pathogenic Frontotemporal dementia 2017-09-13 no assertion criteria provided literature only
VIB Department of Molecular Genetics, University of Antwerp RCV000084519 SCV000116655 not provided not provided no assertion provided not provided

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