ClinVar Miner

Submissions for variant NM_000038.6(APC):c.5604T>A (p.Asp1868Glu)

dbSNP: rs2149944376
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004013824 SCV004825829 uncertain significance Classic or attenuated familial adenomatous polyposis 2023-08-15 criteria provided, single submitter clinical testing

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