ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.837+5G>T

dbSNP: rs1567799952
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Total submissions: 1
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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 RCV001779173 SCV001623554 likely pathogenic Breast-ovarian cancer, familial, susceptibility to, 3 2021-05-10 criteria provided, single submitter curation

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