ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.2634+13G>T

dbSNP: rs1667506255
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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 RCV001190737 SCV001358319 likely benign Hereditary cancer-predisposing syndrome 2018-10-22 criteria provided, single submitter clinical testing
Invitae RCV002069127 SCV002356775 likely benign Hereditary nonpolyposis colorectal neoplasms 2021-05-16 criteria provided, single submitter clinical testing

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