ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.916C>T (p.Gln306Ter)

dbSNP: rs2142409312
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002289403 SCV002580926 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 4 2022-07-29 criteria provided, single submitter clinical testing

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