ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.2211-18T>C

dbSNP: rs1028109019
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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 RCV001185609 SCV001351860 likely benign Hereditary cancer-predisposing syndrome 2019-02-26 criteria provided, single submitter clinical testing
Invitae RCV002068417 SCV002382855 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-03-24 criteria provided, single submitter clinical testing

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