ClinVar Miner

Submissions for variant NM_025077.4(TOE1):c.-44T>G

dbSNP: rs201746729
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000545977 SCV000639313 likely benign Familial adenomatous polyposis 2 2023-11-27 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000583042 SCV000690563 likely benign Hereditary cancer-predisposing syndrome 2017-04-24 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003323599 SCV004029263 uncertain significance not specified 2023-07-04 criteria provided, single submitter clinical testing

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