ClinVar Miner

Submissions for variant NM_002878.4(RAD51D):c.263+1551G>T

dbSNP: rs780006577
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989837 SCV001140424 likely benign Breast-ovarian cancer, familial, susceptibility to, 4 2019-05-28 criteria provided, single submitter clinical testing
Cancer Genomics Group, Japanese Foundation For Cancer Research RCV001030593 SCV001193730 uncertain significance Hereditary breast ovarian cancer syndrome 2019-05-01 criteria provided, single submitter research
Fulgent Genetics, Fulgent Genetics RCV000989837 SCV005641835 uncertain significance Breast-ovarian cancer, familial, susceptibility to, 4 2024-06-13 criteria provided, single submitter clinical testing

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