ClinVar Miner

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

dbSNP: rs1057520840
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003744619 SCV000768363 likely benign Familial adenomatous polyposis 1 2023-04-07 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001191941 SCV001359882 likely benign Hereditary cancer-predisposing syndrome 2019-09-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004004084 SCV004822626 likely benign Classic or attenuated familial adenomatous polyposis 2023-02-24 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004025703 SCV004932133 likely benign Familial adenomatous polyposis 1 2024-02-23 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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