ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1898G>A (p.Gly633Asp) (rs1056085)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000499598 SCV000597143 likely benign not specified 2015-10-06 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000229949 SCV000396869 likely benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000229949 SCV000291067 benign Fanconi anemia 2017-12-05 criteria provided, single submitter clinical testing

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