ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.3777+83_3777+86del

dbSNP: rs773716319
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987108 SCV001136306 benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001675976 SCV001893191 benign not provided 2020-04-01 criteria provided, single submitter clinical testing

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