ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1511-13_1511-11del

dbSNP: rs1418866804
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000584211 SCV000689991 likely benign Hereditary cancer-predisposing syndrome 2017-07-18 criteria provided, single submitter clinical testing
Invitae RCV002061836 SCV002413364 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-01-24 criteria provided, single submitter clinical testing

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