ClinVar Miner

Submissions for variant NM_000038.6(APC):c.730-9T>A

gnomAD frequency: 0.00001  dbSNP: rs780218375
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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 RCV000775123 SCV000909235 uncertain significance Hereditary cancer-predisposing syndrome 2019-02-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002536694 SCV001201697 likely benign Familial adenomatous polyposis 1 2025-01-08 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001192913 SCV001361371 likely benign not specified 2024-12-11 criteria provided, single submitter clinical testing

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