ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.894-10G>A

gnomAD frequency: 0.00001  dbSNP: rs751912856
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000874757 SCV001016980 likely benign Fanconi anemia 2022-10-04 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507530 SCV002801119 likely benign Fanconi anemia complementation group A 2022-02-02 criteria provided, single submitter clinical testing

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