ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.288+37G>A (rs16942918)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242880 SCV000306644 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001636760 SCV001849063 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Nilou-Genome Lab RCV001701961 SCV001933198 benign Fanconi anemia, complementation group I 2021-08-10 criteria provided, single submitter clinical testing

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