ClinVar Miner

Submissions for variant NM_000484.4(APP):c.355+16G>C

dbSNP: rs201791126
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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 RCV003115720 SCV003788324 likely benign Alzheimer disease 2023-02-10 criteria provided, single submitter clinical testing

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