ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2602-18G>C

dbSNP: rs774316884
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002100467 SCV002388979 likely benign Fanconi anemia 2023-12-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002499931 SCV002808097 likely benign Fanconi anemia complementation group A 2021-12-11 criteria provided, single submitter clinical testing

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