ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.220+2432G>A

gnomAD frequency: 0.00001  dbSNP: rs992572864
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
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579906 SCV001808967 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001726606 SCV001965388 likely benign not provided no assertion criteria provided clinical testing

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