ClinVar Miner

Submissions for variant NM_032043.3(BRIP1):c.1795-47G>C

gnomAD frequency: 0.77857  dbSNP: rs4988351
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000250336 SCV000314837 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001711579 SCV001939404 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001711579 SCV005252921 benign not provided criteria provided, single submitter not provided

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