ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2496C>T (p.Phe832=)

dbSNP: rs2039260982
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002205479 SCV002363892 likely benign Fanconi anemia 2021-06-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507916 SCV002804654 likely benign Fanconi anemia complementation group A 2022-05-11 criteria provided, single submitter clinical testing

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