ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.1078G>A (p.Asp360Asn) (rs62063786)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000251165 SCV000306677 benign not specified criteria provided, single submitter clinical testing
Invitae RCV001510736 SCV001717844 benign Frontotemporal dementia 2020-12-08 criteria provided, single submitter clinical testing
GeneDx RCV000084503 SCV001833087 benign not provided 2018-08-11 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 23222517)
VIB Department of Molecular Genetics, University of Antwerp RCV000084503 SCV000116639 not provided not provided no assertion provided not provided
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000251165 SCV001807300 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000251165 SCV001923233 benign not specified no assertion criteria provided clinical testing

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