ClinVar Miner

Submissions for variant NM_021922.2(FANCE):c.266G>T (p.Arg89Leu) (rs45600543)

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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 RCV000121008 SCV000594697 likely benign not specified 2017-05-03 criteria provided, single submitter clinical testing
ITMI RCV000121008 SCV000085176 not provided not specified 2013-09-19 no assertion provided reference population
Invitae RCV000229853 SCV000290609 benign Fanconi anemia, complementation group E 2017-12-15 criteria provided, single submitter clinical testing

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