Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11554495
rs11554495
KRT8
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT

dbSNP: rs57354642
rs57354642
KRT8 ; KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. 12724528

2003
dbSNP: rs57354642
rs57354642
KRT8 ; KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Mutation of human keratin 18 in association with cryptogenic cirrhosis. 9011570

1997
dbSNP: rs57370769
rs57370769
KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. 12724528

2003
dbSNP: rs57370769
rs57370769
KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Mutation of human keratin 18 in association with cryptogenic cirrhosis. 9011570

1997
dbSNP: rs57758506
rs57758506
KRT8 ; KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. 12724528

2003
dbSNP: rs57758506
rs57758506
KRT8 ; KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Mutation of human keratin 18 in association with cryptogenic cirrhosis. 9011570

1997
dbSNP: rs61136606
rs61136606
KRT8 ; KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. 12724528

2003
dbSNP: rs61136606
rs61136606
KRT8 ; KRT18
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Mutation of human keratin 18 in association with cryptogenic cirrhosis. 9011570

1997
dbSNP: rs61710484
rs61710484
KRT8
CUI: C1861556
Disease: Cirrhosis, Familial
Cirrhosis, Familial 		0.700 GeneticVariation UNIPROT Keratin 8 and 18 mutations are risk factors for developing liver disease of multiple etiologies. 12724528

2003