ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.1689T>C (p.Tyr563=) (rs1553367626)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000541980 SCV000625298 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Ambry Genetics RCV000563213 SCV000662322 likely benign Hereditary cancer-predisposing syndrome 2016-11-25 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign
Color RCV000563213 SCV000912997 likely benign Hereditary cancer-predisposing syndrome 2018-10-19 criteria provided, single submitter clinical testing

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