Variant: rs397514767 

    present in Gene: CD59
    present in Chromosome: 11
    Position on Chromosome: 33710247
    Alleles of this Variant: C/T

rs397514767 in CD59 gene and CD59 Deficiency PMID 23149847 2013 CD59 deficiency is associated with chronic hemolysis and childhood relapsing immune-mediated polyneuropathy.

PMID 1382994 1992 Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene.