ClinVar Miner

Submissions for variant NM_003227.4(TFR2):c.671T>G (p.Leu224Arg)

dbSNP: rs1803502704
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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 Medicine and Surgery, University of Milano-Bicocca RCV001250718 SCV001335601 pathogenic Hemochromatosis type 3 2019-01-29 no assertion criteria provided clinical testing

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