ClinVar Miner

Submissions for variant NM_000064.4(C3):c.3908G>A (p.Arg1303His)

dbSNP: rs775015499
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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 RCV000625544 SCV000746039 likely pathogenic Atypical hemolytic-uremic syndrome with C3 anomaly 2017-09-18 no assertion criteria provided clinical testing

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