ClinVar Miner

Submissions for variant NM_000484.4(APP):c.825C>T (p.Thr275=)

dbSNP: rs765151011
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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 RCV002918343 SCV003256536 likely benign Alzheimer disease 2022-10-14 criteria provided, single submitter clinical testing

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