ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.1732+2364C>T

gnomAD frequency: 0.00178  dbSNP: rs187760483
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
Invitae RCV000861531 SCV001001880 benign Frontotemporal dementia 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001692298 SCV001914088 benign not provided 2020-09-23 criteria provided, single submitter clinical testing

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