ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.717C>T (p.Ala239=)

dbSNP: rs63749901
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001457566 SCV001661369 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-17 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007069 SCV004840897 likely benign Lynch syndrome 2023-05-16 criteria provided, single submitter clinical testing

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