ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1958+6T>C

gnomAD frequency: 0.00001  dbSNP: rs368421386
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003743784 SCV000647209 likely benign Familial adenomatous polyposis 1 2023-12-07 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000583831 SCV000686871 likely benign Hereditary cancer-predisposing syndrome 2017-03-07 criteria provided, single submitter clinical testing

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