ClinVar Miner

Submissions for variant NM_001040108.2(MLH3):c.1776A>G (p.Arg592=)

dbSNP: rs745659701
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002078887 SCV002426046 likely benign Colorectal cancer, hereditary nonpolyposis, type 7 2021-11-02 criteria provided, single submitter clinical testing

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