ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.2190G>A (p.Leu730=) (rs864622370)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000204831 SCV000260331 likely benign Hereditary nonpolyposis colon cancer 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000582652 SCV000690053 likely benign Hereditary cancer-predisposing syndrome 2017-09-11 criteria provided, single submitter clinical testing
Ambry Genetics RCV000582652 SCV001175419 likely benign Hereditary cancer-predisposing syndrome 2019-05-22 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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