ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.1623C>T (p.Ser541=) (rs777678406)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000458160 SCV000561458 likely benign Hereditary nonpolyposis colon cancer 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000574333 SCV000669926 likely benign Hereditary cancer-predisposing syndrome 2015-11-14 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Mendelics RCV000986716 SCV001135808 likely benign Hereditary nonpolyposis colorectal cancer type 5 2019-05-28 criteria provided, single submitter clinical testing
Color RCV000574333 SCV001359163 likely benign Hereditary cancer-predisposing syndrome 2018-10-30 criteria provided, single submitter clinical testing

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