ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.2458+8C>T

dbSNP: rs189025757
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001190394 SCV001357859 likely benign Hereditary cancer-predisposing syndrome 2018-10-17 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV001284509 SCV001470342 likely benign not provided 2019-11-18 criteria provided, single submitter clinical testing
Invitae RCV002069116 SCV002321683 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-01-17 criteria provided, single submitter clinical testing

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