ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.862G>A (p.Gly288Arg) (rs76375268)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000635212 SCV000756595 benign Frontotemporal dementia 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001591414 SCV001822873 likely benign not provided 2020-11-21 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001591414 SCV001921967 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001591414 SCV001932899 likely benign not provided no assertion criteria provided clinical testing

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