ClinVar Miner

Submissions for variant NM_022836.4(DCLRE1B):c.807C>T (p.His269=)

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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 RCV003221328 SCV003915697 pathogenic Fanconi anemia complementation group C criteria provided, single submitter clinical testing

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