KRT8, keratin 8, 3856

N. diseases: 166; N. variants: 16
Disease: CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11554495
rs11554495
Entrez Id: 3856
Gene Symbol: KRT8
KRT8
CUI: C1835713
Disease:
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding) 		A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs57758506
rs57758506
Entrez Id: 3856;3875
Gene Symbol: KRT8;KRT18
KRT8;KRT18
CUI: C1835713
Disease:
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO (finding) 		T 0.700 SusceptibilityMutation CLINVAR