ClinVar Miner

Submissions for variant NM_004054.4(C3AR1):c.355_356dup (p.Asp119fs)

dbSNP: rs869312973
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV000210740 SCV000264331 likely pathogenic Hemolytic uremic syndrome, atypical, susceptibility to, 1 2015-11-01 no assertion criteria provided clinical testing

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