ClinVar Miner

Submissions for variant NM_000484.4(APP):c.892G>A (p.Gly298Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004821071 SCV005441972 uncertain significance Cerebral amyloid angiopathy, APP-related 2024-12-19 criteria provided, single submitter clinical testing

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