ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1707G>A (p.Pro569=) (rs141687678)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000859002 SCV000291065 likely benign not provided 2019-01-22 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000233120 SCV000396873 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000500445 SCV000597155 likely benign not specified 2017-04-07 criteria provided, single submitter clinical testing

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