ClinVar Miner

Submissions for variant NM_000038.6(APC):c.934-17del

dbSNP: rs762333924
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000581719 SCV000687184 likely benign Hereditary cancer-predisposing syndrome 2017-03-28 criteria provided, single submitter clinical testing
Preventiongenetics, part of Exact Sciences RCV000679095 SCV000805485 likely benign not provided 2017-04-17 criteria provided, single submitter clinical testing
GeneDx RCV000679095 SCV001910769 benign not provided 2015-05-12 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 23159591)
Invitae RCV003538387 SCV002422503 benign Familial adenomatous polyposis 1 2024-01-29 criteria provided, single submitter clinical testing

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