ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.*394CT[1]

dbSNP: rs546666211
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000350710 SCV000404550 uncertain significance Breast neoplasm 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000396105 SCV000404551 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694343 SCV005192995 uncertain significance not provided criteria provided, single submitter not provided

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