ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.826+5_826+9del (rs797045570)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000192760 SCV000247338 likely pathogenic Fanconi anemia, complementation group A 2015-10-26 criteria provided, single submitter clinical testing

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