ClinVar Miner

Submissions for variant NM_000251.2(MSH2):c.619G>T (p.Ala207Ser) (rs63750913)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000575601 SCV000662290 uncertain significance Hereditary cancer-predisposing syndrome 2019-10-04 criteria provided, single submitter clinical testing Insufficient evidence
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City RCV000723272 SCV000854657 uncertain significance MSH2-related disorder 2018-04-27 no assertion criteria provided clinical testing

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