ClinVar Miner

Submissions for variant NM_000186.4(CFH):c.710_711del (p.Lys236_Cys237insTer)

dbSNP: rs1553273733
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV000505614 SCV000599842 pathogenic Hemolytic uremic syndrome, atypical, susceptibility to, 1 2017-04-20 no assertion criteria provided clinical testing

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