ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.597G>A (p.Glu199=)

dbSNP: rs1425583191
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001432016 SCV001634780 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-11-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006985 SCV004836810 likely benign Lynch syndrome 2023-10-02 criteria provided, single submitter clinical testing

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