ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2628C>A (p.Phe876Leu)

dbSNP: rs368987148
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Hematology, University of Health Sciences RCV000239377 SCV000239244 likely benign Fanconi anemia complementation group A 2014-12-01 no assertion criteria provided research

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