ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.929C>G (p.Thr310Arg) (rs746206527)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000581767 SCV000689932 uncertain significance Hereditary cancer-predisposing syndrome 2018-04-05 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759817 SCV000889411 uncertain significance not provided 2018-07-28 criteria provided, single submitter clinical testing

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