ClinVar Miner

Submissions for variant NM_001283009.2(RTEL1):c.396-43T>C

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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 RCV004560354 SCV005046990 uncertain significance Dyskeratosis congenita, autosomal recessive 5 criteria provided, single submitter clinical testing

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