ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.167T>G (p.Val56Gly)

gnomAD frequency: 0.00033  dbSNP: rs745307359
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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 RCV001779181 SCV001623514 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2021-05-03 criteria provided, single submitter curation
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799083 SCV002043212 uncertain significance Breast and/or ovarian cancer 2019-05-09 criteria provided, single submitter clinical testing

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