ClinVar Miner

Submissions for variant NM_000251.3(MSH2):c.1551A>G (p.Ala517=)

dbSNP: rs753227902
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001180187 SCV001345055 likely benign Hereditary cancer-predisposing syndrome 2019-04-15 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799044 SCV002042094 likely benign Breast and/or ovarian cancer 2019-11-26 criteria provided, single submitter clinical testing

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