ClinVar Miner

Submissions for variant NM_018062.3(FANCL):c.670A>G (p.Thr224Ala) (rs149731356)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000515081 SCV000610020 likely benign not provided 2017-03-29 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000502532 SCV000594733 likely benign not specified 2016-04-20 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000229244 SCV000431335 likely benign Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000229244 SCV000290420 benign Fanconi anemia 2017-04-03 criteria provided, single submitter clinical testing

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