ClinVar Miner

Submissions for variant NM_000484.4(APP):c.663-7T>C

gnomAD frequency: 0.00089  dbSNP: rs183084252
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 RCV001523371 SCV001733066 benign Alzheimer disease 2024-11-06 criteria provided, single submitter clinical testing
Athena Diagnostics RCV004998939 SCV005621673 benign not specified 2024-10-24 criteria provided, single submitter clinical testing

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