ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.180G>A (p.Gln60=)

dbSNP: rs1423192061
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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 RCV001189616 SCV001356928 likely benign Hereditary cancer-predisposing syndrome 2020-04-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003770138 SCV004671021 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2023-05-10 criteria provided, single submitter clinical testing

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