ClinVar Miner

Submissions for variant NM_004972.3(JAK2):c.2048G>C (p.Arg683Thr) (rs1057519722)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Database of Curated Mutations (DoCM) RCV000423852 SCV000504355 pathogenic Lymphoblastic leukemia, acute, with lymphomatous features 2014-10-02 no assertion criteria provided literature only

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