ClinVar Miner

Submissions for variant NM_002875.5(RAD51):c.-98G>C

gnomAD frequency: 0.12401  dbSNP: rs1801320
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001642223 SCV001857577 benign not provided 2018-06-22 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 26117002, 22487057, 24930116, 24604328, 23161237, 11248061, 19606696, 24040396, 21647442, 24859942, 22611952, 16398215, 11535547, 21708019, 20640595, 20623332, 20454923, 20396943, 17999359)
OMIM RCV000014008 SCV000034255 risk factor Breast cancer, susceptibility to, in BRCA1 and BRCA2 carriers 2007-12-01 no assertion criteria provided literature only

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