ClinVar Miner

Submissions for variant NM_000484.4(APP):c.63C>A (p.Pro21=)

gnomAD frequency: 0.00006  dbSNP: rs765279960
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002957312 SCV003269993 likely benign Alzheimer disease 2022-07-20 criteria provided, single submitter clinical testing

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