Variant: rs57758506 

    present in Gene: KRT8;KRT18
    present in Chromosome: 12
    Position on Chromosome: 52949556
    Alleles of this Variant: A/T

rs57758506 in KRT8;KRT18 gene and Cirrhosis, Familial PMID 9011570 1997 Mutation of human keratin 18 in association with cryptogenic cirrhosis.

PMID 12724528 2003 Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.