Disease: Liver Failure ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Liver Failure
CUI: C0085605
Disease: Liver Failure
0.010 GeneticVariation BEFREE A homozygous mutation located at Chr17: 62492543G>A in POLG2, resulting in R182W substitution in p55, was previously identified to cause mtDNA depletion and fatal hepatic liver failure. 30157269 2018