ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.848G>A (p.Gly283Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005012251 SCV005642301 uncertain significance Frontotemporal dementia; Parkinson disease, late-onset; Progressive supranuclear palsy-parkinsonism syndrome; Pick disease; Supranuclear palsy, progressive, 1 2024-03-19 criteria provided, single submitter clinical testing

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