ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1958+27del

dbSNP: rs1402242990
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662732 SCV000785501 likely benign Familial adenomatous polyposis 1 2017-08-22 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV003316783 SCV004020034 benign Familial adenomatous polyposis 1 2023-02-13 criteria provided, single submitter clinical testing This variant is considered benign. This variant is intronic and is not expected to impact mRNA splicing.

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