ClinVar Miner

Submissions for variant NM_000484.4(APP):c.2211+11T>C

dbSNP: rs2037709275
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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 RCV002715042 SCV002989409 likely benign Alzheimer disease 2022-04-15 criteria provided, single submitter clinical testing

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