ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.572-1G>T

dbSNP: rs1413872299
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Hereditary Cancer Group, L’Institut d'Investigació Biomèdica de Bellvitge RCV001779199 SCV001623533 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 3 2021-05-03 criteria provided, single submitter curation
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003492253 SCV004239991 likely pathogenic Breast and/or ovarian cancer 2023-04-06 criteria provided, single submitter clinical testing

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