ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.1334G>C (p.Ser445Thr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003330202 SCV004037219 uncertain significance Lynch syndrome 5 2023-03-14 criteria provided, single submitter clinical testing

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