ClinVar Miner

Submissions for variant NM_000038.6(APC):c.136-13T>G

dbSNP: rs1340361442
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001175821 SCV001339552 likely benign Hereditary cancer-predisposing syndrome 2017-02-15 criteria provided, single submitter clinical testing
Invitae RCV003537490 SCV004368389 likely benign Familial adenomatous polyposis 1 2023-11-24 criteria provided, single submitter clinical testing

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