ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.523-37TTGTTT[2]

dbSNP: rs530849202
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002097355 SCV002381157 likely benign Fanconi anemia 2024-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498316 SCV002808541 likely benign Fanconi anemia complementation group A 2022-03-21 criteria provided, single submitter clinical testing

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