ClinVar Miner

Submissions for variant NM_004526.4(MCM2):c.920G>C (p.Arg307Pro)

dbSNP: rs2074353310
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics and Genomics, Karolinska University Hospital RCV001269624 SCV001449742 likely pathogenic not provided 2019-04-30 criteria provided, single submitter clinical testing

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