ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.966-8T>G

gnomAD frequency: 0.00001  dbSNP: rs1181139153
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000527554 SCV000660418 likely benign Fanconi anemia complementation group O 2023-11-20 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002483521 SCV002784754 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 3; Fanconi anemia complementation group O 2021-10-27 criteria provided, single submitter clinical testing

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