ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.904-20C>A

dbSNP: rs2091529783
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001190564 SCV001358074 likely benign Hereditary cancer-predisposing syndrome 2019-07-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560085 SCV003467771 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2024-02-29 criteria provided, single submitter clinical testing

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