Variant: rs121913051 

    present in Gene: CFH
    present in Chromosome: 1
    Position on Chromosome: 196747260
    Alleles of this Variant: C/G;T

rs121913051 in CFH gene and HEMOLYTIC UREMIC SYNDROME, ATYPICAL, SUSCEPTIBILITY TO, 1 PMID 19846853 2009 Atypical hemolytic-uremic syndrome.

PMID 19821824 2010 Clinical practice guidelines for the management of atypical haemolytic uraemic syndrome in the United Kingdom.