Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16851720
rs16851720
0.810 GeneticVariation BEFREE Our study showed that PNPLA3 rs738409 and RNF7 rs16851720 confer an increased risk of developing liver fibrosis and cirrhosis in this Eastern European population, while the MERTK and PCSK7 SNPs are not associated with these conditions. 28338112

2017

dbSNP: rs4374383
rs4374383
0.810 GeneticVariation BEFREE We evaluated the associations between the PNPLA3 (rs738409), RNF7 (rs16851720), MERTK (rs4374383) and PCSK7 (rs236918) variants and liver fibrosis and cirrhosis in a series of consecutive patients recruited at the Department of Gastroenterology, Lithuanian University of Health Sciences Hospital, during the period 2012-2015. 28338112

2017

dbSNP: rs16851720
rs16851720
C 0.810 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs16851720
rs16851720
C 0.810 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs4374383
rs4374383
A 0.810 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs4374383
rs4374383
A 0.810 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs2629751
rs2629751
G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs2629751
rs2629751
G 0.800 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs9380516
rs9380516
T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs9380516
rs9380516
T 0.800 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012

dbSNP: rs2896019
rs2896019
G 0.700 GeneticVariation GWASCAT Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan. 23535911

2013

dbSNP: rs1227756
rs1227756
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs2645424
rs2645424
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs2710833
rs2710833
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs343064
rs343064
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs643608
rs643608
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs6487679
rs6487679
G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs6591182
rs6591182
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs887304
rs887304
A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010

dbSNP: rs1396171148
rs1396171148
G 0.700 CausalMutation CLINVAR

dbSNP: rs1419129874
rs1419129874
G 0.700 CausalMutation CLINVAR

dbSNP: rs1466642025
rs1466642025
G 0.700 CausalMutation CLINVAR

dbSNP: rs1553553086
rs1553553086
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553554543
rs1553554543
C 0.700 CausalMutation CLINVAR

dbSNP: rs367956522
rs367956522
C 0.700 CausalMutation CLINVAR