ClinVar Miner

Submissions for variant NM_000038.6(APC):c.933+19C>A

dbSNP: rs778599778
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581372 SCV000687181 likely benign Hereditary cancer-predisposing syndrome 2017-06-12 criteria provided, single submitter clinical testing
Counsyl RCV000663201 SCV000786379 likely benign Familial adenomatous polyposis 1 2018-04-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000663201 SCV002443487 likely benign Familial adenomatous polyposis 1 2024-11-17 criteria provided, single submitter clinical testing

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