ClinVar Miner

Submissions for variant NM_005475.3(SH2B3):c.603_607del (p.Arg202fs)

dbSNP: rs587776885
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023397 SCV000044688 pathogenic Primary myelofibrosis 2010-08-12 no assertion criteria provided literature only

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