ClinVar Miner

Submissions for variant NM_000251.1(MSH2):c.-823_1076+5984del

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000075991 SCV000106980 pathogenic Lynch syndrome 2013-09-05 reviewed by expert panel research Large deletion
OMIM RCV000001841 SCV000021997 pathogenic Lynch syndrome 1 2004-02-11 no assertion criteria provided literature only
GeneReviews RCV000001841 SCV002054073 not provided Lynch syndrome 1 no assertion provided literature only

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