ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3647-15A>G

dbSNP: rs371171254
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001187643 SCV001354497 likely benign Hereditary cancer-predisposing syndrome 2023-05-24 criteria provided, single submitter clinical testing
Invitae RCV002057038 SCV002346947 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-10-28 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV003997047 SCV004830257 likely benign Lynch syndrome 2023-06-08 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000202245 SCV000257269 uncertain significance not specified no assertion criteria provided research

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