ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2679G>A (p.Trp893Ter)

dbSNP: rs2143288874
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Istanbul Faculty of Medicine, Istanbul University RCV002254009 SCV002524167 pathogenic Fanconi anemia complementation group A 2022-06-06 no assertion criteria provided clinical testing

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