ClinVar Miner

Submissions for variant NM_001128425.2(MUTYH):c.36+214G>C

gnomAD frequency: 0.00096  dbSNP: rs568514678
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000986308 SCV001135271 likely benign Familial adenomatous polyposis 2 2019-05-28 criteria provided, single submitter clinical testing
Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C. RCV003315256 SCV004014930 likely benign Hereditary cancer-predisposing syndrome 2023-03-21 criteria provided, single submitter clinical testing

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