ClinVar Miner

Submissions for variant NM_000249.3(MLH1):c.2198A>G (p.His733Arg) (rs770579083)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000571053 SCV000662083 uncertain significance Hereditary cancer-predisposing syndrome 2016-09-19 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
Color RCV000571053 SCV000908657 uncertain significance Hereditary cancer-predisposing syndrome 2018-07-12 criteria provided, single submitter clinical testing

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