ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.2636+11C>G

dbSNP: rs1596307878
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000989375 SCV001139672 likely benign Fanconi anemia complementation group A 2019-05-28 criteria provided, single submitter clinical testing
Invitae RCV002067584 SCV002417301 likely benign Fanconi anemia 2020-11-15 criteria provided, single submitter clinical testing

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