ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.*1255AG[1]

dbSNP: rs886053209
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000353542 SCV000404536 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000260982 SCV000404537 uncertain significance Breast neoplasm 2016-06-14 criteria provided, single submitter clinical testing

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