ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.263+1474C>T

gnomAD frequency: 0.00016  dbSNP: rs201720876
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583476 SCV000691313 likely benign Hereditary cancer-predisposing syndrome 2015-04-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002292569 SCV002585641 likely benign not provided 2025-05-01 criteria provided, single submitter clinical testing RAD51D: BP4, BS1
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005231132 SCV005877527 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-05-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003945368 SCV004764385 likely benign RAD51D-related disorder 2019-04-19 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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