ClinVar Miner

Submissions for variant NM_000038.6(APC):c.3904C>T (p.Leu1302=)

dbSNP: rs2149901708
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV004572062 SCV002420928 likely benign Familial adenomatous polyposis 1 2021-10-28 criteria provided, single submitter clinical testing

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