ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.668-20dup

dbSNP: rs2142419061
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002099137 SCV002440059 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2021-12-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV002099137 SCV006094053 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 intronic and is not expected to impact mRNA splicing.

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