ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3636G>T (p.Val1212=) (rs1363247790)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000541872 SCV000624893 likely benign Hereditary nonpolyposis colon cancer 2017-06-05 criteria provided, single submitter clinical testing
Mendelics RCV000708892 SCV000837920 uncertain significance Lynch syndrome 2018-07-02 criteria provided, single submitter clinical testing
Mendelics RCV000986739 SCV001135844 likely benign Hereditary nonpolyposis colorectal cancer type 5 2019-05-28 criteria provided, single submitter clinical testing
Ambry Genetics RCV001020774 SCV001182297 likely benign Hereditary cancer-predisposing syndrome 2019-09-21 criteria provided, single submitter clinical testing In silico models in agreement (benign);Synonymous alterations with insufficient evidence to classify as benign

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