ClinVar Miner

Submissions for variant NM_000484.4(APP):c.1926C>T (p.Ala642=)

gnomAD frequency: 0.00001  dbSNP: rs778792696
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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 RCV003622112 SCV004532115 likely benign Alzheimer disease 2023-06-15 criteria provided, single submitter clinical testing

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