ClinVar Miner

Submissions for variant NM_000038.6(APC):c.6093T>C (p.Ser2031=)

dbSNP: rs1580667476
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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 RCV002550539 SCV001682984 likely benign Familial adenomatous polyposis 1 2018-11-06 criteria provided, single submitter clinical testing

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