ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2308G>T (p.Gly770Cys)

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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 RCV003229514 SCV003925764 likely pathogenic Lynch syndrome 1 no assertion criteria provided clinical testing Endometrial cancer and colorectal cancer, patient mother had breast cancer

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