ClinVar Miner

Submissions for variant NM_000484.4(APP):c.1809C>T (p.Thr603=)

gnomAD frequency: 0.00004  dbSNP: rs150151009
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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 RCV002122128 SCV002394729 likely benign Alzheimer disease 2024-11-27 criteria provided, single submitter clinical testing

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