ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1485A>T (p.Thr495=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine, Sinai Health System RCV005362152 SCV005921053 likely benign Lynch syndrome 1; Muir-Torré syndrome; Mismatch repair cancer syndrome 2 2019-10-24 criteria provided, single submitter clinical testing

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