ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4241C>T (p.Pro1414Leu) (rs140892471)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194698 SCV000248933 likely benign not specified 2015-04-12 criteria provided, single submitter clinical testing
Invitae RCV000465744 SCV000558627 benign Fanconi anemia 2017-12-04 criteria provided, single submitter clinical testing

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