Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs738409
rs738409
0.030 GeneticVariation BEFREE High frequency of the PNPLA3 rs738409 [G] single-nucleotide polymorphism in Hmong individuals as a potential basis for a predisposition to chronic liver disease. 29578593

2018

dbSNP: rs738409
rs738409
0.030 GeneticVariation BEFREE The PNPLA3 I148M substitution is a major common genetic determinant of hepatic fat content and progression to chronic liver disease. 26355465

2016

dbSNP: rs738409
rs738409
0.030 GeneticVariation BEFREE Our results indicate that the PNPLA3 I148M variant is relevant for the retinyl-palmitate content in human liver, providing a possible link to chronic liver disease. 26439088

2015