ClinVar Miner

Submissions for variant NM_002875.5(RAD51):c.772G>A (p.Glu258Lys)

dbSNP: rs1555429629
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Undiagnosed Diseases Network, NIH RCV000626039 SCV000746654 likely pathogenic Fanconi anemia complementation group R 2017-12-12 criteria provided, single submitter clinical testing
Daryl Scott Lab, Baylor College of Medicine RCV000626039 SCV002515372 likely pathogenic Fanconi anemia complementation group R 2022-02-01 criteria provided, single submitter clinical testing

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