ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.706-5_706-4dup

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002466016 SCV002760382 benign not specified 2023-08-15 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150570 SCV003838394 likely benign Breast and/or ovarian cancer 2022-04-29 criteria provided, single submitter clinical testing
Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C. RCV003482168 SCV004227995 likely benign Hereditary cancer-predisposing syndrome 2023-10-31 criteria provided, single submitter clinical testing

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