ClinVar Miner

Submissions for variant NM_000038.6(APC):c.1626+8T>G

dbSNP: rs773400235
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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 RCV000775133 SCV000909249 likely benign Hereditary cancer-predisposing syndrome 2017-01-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV004561758 SCV001077988 likely benign Familial adenomatous polyposis 1 2024-10-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV004561758 SCV004931155 likely benign Familial adenomatous polyposis 1 2024-03-06 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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