ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3652-70_3652-69del

dbSNP: rs11321073
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989377 SCV001139674 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001615097 SCV001839651 benign not provided 2019-08-19 criteria provided, single submitter clinical testing

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