ClinVar Miner

Submissions for variant NM_000484.4(APP):c.462C>T (p.Ala154=)

gnomAD frequency: 0.00008  dbSNP: rs200398369
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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 RCV002905034 SCV003267008 likely benign Alzheimer disease 2023-06-20 criteria provided, single submitter clinical testing

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