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 |
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 |
rs16851720
|
|
C |
0.810 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs16851720
|
|
C |
0.810 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs4374383
|
|
A |
0.810 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs4374383
|
|
A |
0.810 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs2629751
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs2629751
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs9380516
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
rs9380516
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
|
22841784 |
2012 |
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 |
rs1227756
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs2645424
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs2710833
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs343064
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs643608
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs6487679
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs6591182
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs887304
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.
|
20708005 |
2010 |
rs1396171148
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1419129874
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1466642025
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1553553086
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1553554543
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs367956522
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|