ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.2538G>T (p.Gln846His)

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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 RCV005399923 SCV006056462 uncertain significance Lynch syndrome 1; Muir-Torré syndrome; Mismatch repair cancer syndrome 2 2020-11-26 criteria provided, single submitter clinical testing

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