ClinVar Miner

Submissions for variant NM_001113378.2(FANCI):c.3059-11C>T

dbSNP: rs2054667046
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002257257 SCV002529835 uncertain significance Fanconi anemia 2022-03-08 criteria provided, single submitter curation
Invitae RCV002257257 SCV004638968 likely benign Fanconi anemia 2024-01-05 criteria provided, single submitter clinical testing

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