ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.628-8C>G

dbSNP: rs767991179
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001707752 SCV000718498 likely benign not provided 2021-05-14 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000777253 SCV000912954 likely benign Hereditary cancer-predisposing syndrome 2023-06-08 criteria provided, single submitter clinical testing
Invitae RCV000809810 SCV000949986 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-11-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002510 SCV004827099 likely benign Lynch syndrome 2023-06-26 criteria provided, single submitter clinical testing

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