ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.220+18C>T (rs75242405)

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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 RCV000244111 SCV000306673 benign not specified criteria provided, single submitter clinical testing
Invitae RCV001510733 SCV001717841 benign Frontotemporal dementia 2020-12-02 criteria provided, single submitter clinical testing
GeneDx RCV001610607 SCV001834618 benign not provided 2018-08-11 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV000244111 SCV001808923 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000244111 SCV001926000 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000244111 SCV001967691 benign not specified no assertion criteria provided clinical testing

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