Variant: rs1060499624 

    present in Gene: RANBP2
    present in Chromosome: 2
    Position on Chromosome: 108765788
    Alleles of this Variant: C/G

rs1060499624 in RANBP2 gene and ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 PMID 19118815 2009 Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.

PMID 2759111 1989 Haemorheologic studies in patients with reduced coronary vasodilator capacity but normal coronary angiogram (syndrome X).