ClinVar Miner

Submissions for variant NM_000135.2(FANCA):c.-138_-126dup

dbSNP: rs11275235
Minimum review status: Collection method:
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ClinVar version:
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 RCV000192687 SCV000247335 uncertain significance not specified 2015-04-03 criteria provided, single submitter clinical testing
GeneDx RCV001651056 SCV001870653 benign not provided 2019-01-10 criteria provided, single submitter clinical testing

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