ClinVar Miner

Submissions for variant NM_000038.6(APC):c.532-7G>C

dbSNP: rs1057520840
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001720052 SCV000518362 likely benign not provided 2019-12-03 criteria provided, single submitter clinical testing
Invitae RCV002230013 SCV000562582 likely benign Familial adenomatous polyposis 1 2023-08-07 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000579458 SCV000681732 likely benign Hereditary cancer-predisposing syndrome 2017-07-06 criteria provided, single submitter clinical testing

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