ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.556C>A (p.Arg186=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Myriad Genetics, Inc. RCV005426672 SCV006093707 benign Breast-ovarian cancer, familial, susceptibility to, 4 2025-02-24 criteria provided, single submitter clinical testing This variant is considered benign. This variant is a silent/synonymous amino acid change and it is not expected to impact splicing.

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