ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.261-20G>C

dbSNP: rs1382008214
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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 RCV001190048 SCV001357461 likely benign Hereditary cancer-predisposing syndrome 2019-02-25 criteria provided, single submitter clinical testing
GeneDx RCV001712880 SCV001940385 benign not provided 2015-03-04 criteria provided, single submitter clinical testing
Invitae RCV002069102 SCV002385479 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-01-14 criteria provided, single submitter clinical testing

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