ClinVar Miner

Submissions for variant NM_016835.4(MAPT):c.1866T>C (p.Ser622=) (rs63750568)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989937 SCV001140678 pathogenic Frontotemporal dementia 2019-05-28 criteria provided, single submitter clinical testing
VIB Department of Molecular Genetics, University of Antwerp RCV000084531 SCV000116667 not provided not provided no assertion provided not provided

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