ClinVar Miner

Submissions for variant NM_025077.4(TOE1):c.-43C>A

dbSNP: rs766584437
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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 RCV000772838 SCV000906220 likely benign Hereditary cancer-predisposing syndrome 2018-05-17 criteria provided, single submitter clinical testing
Invitae RCV000937891 SCV001083685 likely benign Familial adenomatous polyposis 2 2023-12-18 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003387925 SCV004099704 likely benign not specified 2023-09-01 criteria provided, single submitter clinical testing

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