ClinVar Miner

Submissions for variant NM_000484.4(APP):c.741C>T (p.Asp247=)

gnomAD frequency: 0.00106  dbSNP: rs148832151
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
Invitae RCV000872725 SCV001014584 benign Alzheimer disease 2023-10-04 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV001288439 SCV001475535 benign not specified 2019-11-12 criteria provided, single submitter clinical testing

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