ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.841G>T (p.Ala281Ser)

dbSNP: rs1321460540
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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 RCV000700976 SCV000829756 likely benign Frontotemporal dementia 2024-02-17 criteria provided, single submitter clinical testing

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