ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.915A>C (p.Ala305=) (rs757483245)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000226255 SCV000284194 likely benign Hereditary nonpolyposis colorectal neoplasms 2019-12-31 criteria provided, single submitter clinical testing
Color RCV000774559 SCV000908285 likely benign Hereditary cancer-predisposing syndrome 2018-04-26 criteria provided, single submitter clinical testing
Ambry Genetics RCV000774559 SCV001180224 likely benign Hereditary cancer-predisposing syndrome 2018-04-16 criteria provided, single submitter clinical testing Synonymous alterations with insufficient evidence to classify as benign

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