ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.2128A>G (p.Asn710Asp)

dbSNP: rs1559595840
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002168468 SCV002421619 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-08-10 criteria provided, single submitter clinical testing
Baylor Genetics RCV003464405 SCV004190657 uncertain significance Colorectal cancer, hereditary nonpolyposis, type 2 2023-08-04 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004005416 SCV004834488 uncertain significance Lynch syndrome 2024-01-11 criteria provided, single submitter clinical testing

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