ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2559_2564del (p.Asp854_Thr855del)

dbSNP: rs2143308232
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dept. of Cytogenetics, ICMR- National Institute of Immunohaematology RCV001615369 SCV001832561 uncertain significance Fanconi anemia criteria provided, single submitter clinical testing

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