ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.2058C>A (p.Ile686=)

dbSNP: rs1242136178
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000985783 SCV001134302 uncertain significance not provided 2019-07-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002067570 SCV002419040 likely benign Hereditary nonpolyposis colorectal neoplasms 2021-09-26 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004004414 SCV004843262 likely benign Lynch syndrome 2023-08-28 criteria provided, single submitter clinical testing

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