ClinVar Miner

Submissions for variant NM_000038.6(APC):c.933+15C>T

dbSNP: rs752050909
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000679094 SCV000805484 likely benign not provided 2017-12-20 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000775124 SCV000909237 likely benign Hereditary cancer-predisposing syndrome 2018-09-25 criteria provided, single submitter clinical testing
Invitae RCV003768033 SCV002442343 likely benign Familial adenomatous polyposis 1 2023-12-17 criteria provided, single submitter clinical testing

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