ClinVar Miner

Submissions for variant NM_000038.6(APC):c.6957A>G (p.Arg2319=)

dbSNP: rs1580676744
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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 RCV004563585 SCV001623739 likely benign Familial adenomatous polyposis 1 2018-07-26 criteria provided, single submitter clinical testing

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