ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.793-9T>C (rs757500718)

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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 RCV000501039 SCV000594649 uncertain significance not specified 2017-03-28 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000363325 SCV000399876 uncertain significance Fanconi anemia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000363325 SCV000558866 likely benign Fanconi anemia 2016-07-24 criteria provided, single submitter clinical testing

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