ClinVar Miner

List of variants reported as risk factor for Atypical hemolytic-uremic syndrome 1

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_000186.3(CFH):c.2697T>A (p.Tyr899Ter) rs121913057
NM_000186.3(CFH):c.3514G>T (p.Glu1172Ter) rs121913060
NM_000186.3(CFH):c.3566T>G (p.Leu1189Arg) rs121913055
NM_000186.3(CFH):c.3572C>T (p.Ser1191Leu) rs460897
NM_000186.3(CFH):c.3592G>T (p.Glu1198Ter) rs121913063
NM_000186.3(CFH):c.3628C>T (p.Arg1210Cys) rs121913059
NM_000186.3(CFH):c.3643C>G (p.Arg1215Gly) rs121913051
NM_000186.3(CFH):c.3677_*4del (p.Pro1226_Ter1232delinsXaa) rs796052136
NM_000186.3(CFH):c.83_86del (p.Arg28fs) rs796052137

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.