ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.*241dup

dbSNP: rs55661512
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services,Illumina RCV000301434 SCV000403496 benign MAPT-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001643010 SCV001856709 benign not provided 2018-09-28 criteria provided, single submitter clinical testing

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