ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.2034C>T (p.Asn678=)

gnomAD frequency: 0.00003  dbSNP: rs779043983
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001430919 SCV001633668 likely benign Frontotemporal dementia 2023-12-11 criteria provided, single submitter clinical testing

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