ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1759+11_1759+15del

dbSNP: rs878853805
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000234476 SCV000284122 likely benign Lynch syndrome 2016-01-15 criteria provided, single submitter clinical testing
Invitae RCV003593943 SCV004285585 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-02-14 criteria provided, single submitter clinical testing

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