ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.2406T>C (p.Asn802=)

gnomAD frequency: 0.00009  dbSNP: rs115381139
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000873732 SCV001015787 benign Frontotemporal dementia 2024-11-21 criteria provided, single submitter clinical testing

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