ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2779-5C>G

dbSNP: rs753286882
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002157946 SCV002425688 likely benign Fanconi anemia 2022-05-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494323 SCV002796130 likely benign Fanconi anemia complementation group A 2021-11-10 criteria provided, single submitter clinical testing

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