ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.564_567del (p.Val189fs)

dbSNP: rs2142428876
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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 RCV001838814 SCV001806921 likely pathogenic Deleterious RAD51D Gene Mutation 2021-08-24 criteria provided, single submitter research

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