ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.1377C>T (p.Asp459=)

gnomAD frequency: 0.00003  dbSNP: rs371173110
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002548293 SCV001110857 likely benign Frontotemporal dementia 2022-07-08 criteria provided, single submitter clinical testing

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