ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.2128_2131dup (p.Ser711Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Personalized Medicine Clinic, Tartu University Hospital RCV003229526 SCV003925772 likely pathogenic Lynch syndrome 1 no assertion criteria provided clinical testing Colorectal cancer in anamnesis. Mother and sister also had colorectal cancer at an early age

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