|
rs4780355
|
SOCS1;RMI2;LOC105371082
|
Psoriasis
|
T |
0.800 |
GeneticVariation |
GWASDB |
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
|
22482804 |
2012 |
|
rs4780355
|
SOCS1;RMI2;LOC105371082
|
Psoriasis
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
|
22482804 |
2012 |
|
rs11549428
|
SOCS1;RMI2;LOC105371082
|
Eosinophil count procedure
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
|
rs193778
|
SOCS1;RMI2;LOC105371082
|
Diabetes Mellitus, Insulin-Dependent
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers.
|
25751624 |
2015 |
|
rs188754154
|
SOCS1;RMI2;LOC105371082
|
Primary biliary cirrhosis
|
|
0.700 |
GeneticVariation |
GWASDB |
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
|
22961000 |
2012 |
|
rs4780355
|
SOCS1;RMI2;LOC105371082
|
Primary biliary cirrhosis
|
|
0.700 |
GeneticVariation |
GWASDB |
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
|
22961000 |
2012 |
|
rs4780355
|
SOCS1;RMI2;LOC105371082
|
Crohn Disease
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
|
22482804 |
2012 |
|
rs243330
|
SOCS1;RMI2;LOC105371082
|
Obesity
|
|
0.020 |
GeneticVariation |
BEFREE |
The polymorphism of the <i>SOCS1</i> gene (rs243330, -1656G>A) is associated with obesity and glucose sensitivity.
|
31717271 |
2019 |
|
rs243330
|
SOCS1;RMI2;LOC105371082
|
Obesity
|
|
0.020 |
GeneticVariation |
BEFREE |
In a second study (n = 4625 NGT subjects), significant associations of both the rs33977706 and the rs243330 (-1656G > A) variants to obesity were found (p = 0.047 and p = 0.015) respectively.
|
19215277 |
2009 |
|
rs243330
|
SOCS1;RMI2;LOC105371082
|
Atherosclerosis
|
|
0.010 |
GeneticVariation |
BEFREE |
Under heterozygous model, the rs33932899 and rs243330 were significantly associated with ischemic stroke subtypes by atherosclerosis (p = 0.038, p = 0.048, respectively).
|
27216615 |
2016 |
|
rs243330
|
SOCS1;RMI2;LOC105371082
|
Arteriosclerosis
|
|
0.010 |
GeneticVariation |
BEFREE |
Under heterozygous model, the rs33932899 and rs243330 were significantly associated with ischemic stroke subtypes by atherosclerosis (p = 0.038, p = 0.048, respectively).
|
27216615 |
2016 |
|
rs33932899
|
SOCS1;RMI2;LOC105371082
|
Atherosclerosis
|
|
0.010 |
GeneticVariation |
BEFREE |
Under heterozygous model, the rs33932899 and rs243330 were significantly associated with ischemic stroke subtypes by atherosclerosis (p = 0.038, p = 0.048, respectively).
|
27216615 |
2016 |
|
rs33932899
|
SOCS1;RMI2;LOC105371082
|
Arteriosclerosis
|
|
0.010 |
GeneticVariation |
BEFREE |
Under heterozygous model, the rs33932899 and rs243330 were significantly associated with ischemic stroke subtypes by atherosclerosis (p = 0.038, p = 0.048, respectively).
|
27216615 |
2016 |
|
rs243330
|
SOCS1;RMI2;LOC105371082
|
Acute Chest Syndrome
|
|
0.010 |
GeneticVariation |
BEFREE |
On the other hand, under co-dominant and heterozygous models, the -1656 G/A (rs243330) SNP was associated with increased risk of ACS (OR=1.47, P(Co-dom)=0.038 and OR=1.50, P(Het)=0.013, respectively).
|
24997329 |
2014 |
|
rs33932899
|
SOCS1;RMI2;LOC105371082
|
Hepatitis B
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotype GC and allele C of rs33932899 were significantly less frequent in HBV patients than controls (pc < 0.001 and p < 0.001, respectively).
|
24768946 |
2014 |
|
rs33932899
|
SOCS1;RMI2;LOC105371082
|
Acute Chest Syndrome
|
|
0.010 |
GeneticVariation |
BEFREE |
Finally, under co-dominant and heterozygous models, the +1125 G/C (rs33932899) SNP was associated with increased risk of ACS (OR=1.54, P(Co-dom)=0.006, OR=1.58, P(Het)=0.012, respectively).
|
24997329 |
2014 |
|
rs33977706
|
SOCS1;RMI2;LOC105371082
|
Acute Chest Syndrome
|
|
0.010 |
GeneticVariation |
BEFREE |
Moreover, under co-dominant, dominant, and heterozygous models, the -820T/G (rs33977706) SNP was associated with increased risk of ACS (OR=1.59, P(Co-dom)=0.03, OR=1.48, P(Dom)=0.028 and OR=1.61, P(Het)=0.01).
|
24997329 |
2014 |
|
rs33977706
|
SOCS1;RMI2;LOC105371082
|
Obesity
|
|
0.010 |
GeneticVariation |
BEFREE |
In a second study (n = 4625 NGT subjects), significant associations of both the rs33977706 and the rs243330 (-1656G > A) variants to obesity were found (p = 0.047 and p = 0.015) respectively.
|
19215277 |
2009 |