ClinVar Miner

Submissions for variant NM_058216.3(RAD51C):c.1000del (p.Glu334fs)

dbSNP: rs1567817415
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709518 SCV000839342 likely pathogenic Hereditary breast ovarian cancer syndrome 2018-07-02 criteria provided, single submitter clinical testing
Mendelics RCV000989966 SCV001140728 likely pathogenic Fanconi anemia complementation group O 2019-05-28 criteria provided, single submitter clinical testing

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