ClinVar Miner

Submissions for variant NM_000484.4(APP):c.866-16C>A

gnomAD frequency: 0.00009  dbSNP: rs201470897
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002776490 SCV003030708 likely benign Alzheimer disease 2025-01-15 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005059045 SCV005726489 likely benign not specified 2024-11-12 criteria provided, single submitter clinical testing

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