ClinVar Miner

Submissions for variant NM_153609.3(TMPRSS6):c.1795C>T (p.Arg599Ter) (rs137853123)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000001473 SCV000021628 pathogenic Microcytic anemia 2008-09-01 no assertion criteria provided literature only
NIHR Bioresource Rare Diseases, University of Cambridge RCV000001473 SCV001162263 likely pathogenic Microcytic anemia no assertion criteria provided research

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