ClinVar Miner

Submissions for variant NM_000186.4(CFH):c.3542T>C (p.Leu1181Ser)

dbSNP: rs1573087200
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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 RCV000787023 SCV000925933 likely pathogenic Hemolytic uremic syndrome, atypical, susceptibility to, 1 2019-02-28 no assertion criteria provided clinical testing

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