Variant: rs57370769 

    present in Gene: KRT18
    present in Chromosome: 12
    Position on Chromosome: 52952188
    Alleles of this Variant: G/A

rs57370769 in KRT18 gene and Cirrhosis, Familial PMID 12724528 2003 Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies.

PMID 9011570 1997 Mutation of human keratin 18 in association with cryptogenic cirrhosis.