ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.-238A>T

gnomAD frequency: 0.00757  dbSNP: rs188262287
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662967 SCV000785946 benign Breast-ovarian cancer, familial, susceptibility to, 4 2018-01-22 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004709586 SCV005246799 benign not provided criteria provided, single submitter not provided

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