ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1732-7T>C

dbSNP: rs745745276
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000554927 SCV000625095 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-12-22 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000583602 SCV000689836 likely benign Hereditary cancer-predisposing syndrome 2016-09-27 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV002476085 SCV002774178 likely benign not provided 2021-06-23 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003715 SCV004822624 likely benign Lynch syndrome 2023-11-02 criteria provided, single submitter clinical testing

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