CTNNBL1, catenin beta like 1, 56259

N. diseases: 68; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16986890
rs16986890
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C1285654
Disease:
Memory performance
0.700 GeneticVariation GWASDB A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. 22105620 2013
dbSNP: rs6020395
rs6020395
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C1285654
Disease:
Memory performance
0.700 GeneticVariation GWASDB A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. 22105620 2013
dbSNP: rs6020712
rs6020712
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C1285654
Disease:
Memory performance
0.700 GeneticVariation GWASDB A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. 22105620 2013
dbSNP: rs9679781
rs9679781
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C1285654
Disease:
Memory performance
0.700 GeneticVariation GWASDB A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. 22105620 2013
dbSNP: rs16986921
rs16986921
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0578022
Disease:
Finding of body mass index
0.700 GeneticVariation GWASDB Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. 18325910 2008
dbSNP: rs16986921
rs16986921
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.700 GeneticVariation GWASDB Multiple loci identified in a genome-wide association study of prostate cancer. 18264096 2008
dbSNP: rs16986921
rs16986921
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0005893
Disease:
Body mass index procedure
0.700 GeneticVariation GWASDB Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. 18325910 2008
dbSNP: rs6013029
rs6013029
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0578022
Disease:
Finding of body mass index
0.700 GeneticVariation GWASDB Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. 18325910 2008
dbSNP: rs6013029
rs6013029
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.700 GeneticVariation GWASDB Multiple loci identified in a genome-wide association study of prostate cancer. 18264096 2008
dbSNP: rs6013029
rs6013029
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0005893
Disease:
Body mass index procedure
0.700 GeneticVariation GWASDB The SNP rs6013029 minor allele T confers an average increase in BMI and fat mass of 2.67 kg/m(2) and 5.96 kg, respectively, compared with the alternative allele G. We further genotyped the five most significant CTNNBL1 SNPs in a French case-control sample comprising 896 class III obese adults (BMI > or = 40 kg/m(2)) and 2916 lean adults (BMI < 25 kg/m(2)). 18325910 2008
dbSNP: rs6020712
rs6020712
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0578022
Disease:
Finding of body mass index
0.700 GeneticVariation GWASDB Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. 18325910 2008
dbSNP: rs6020712
rs6020712
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0005893
Disease:
Body mass index procedure
0.700 GeneticVariation GWASDB Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. 18325910 2008
dbSNP: rs6020712
rs6020712
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.700 GeneticVariation GWASDB Multiple loci identified in a genome-wide association study of prostate cancer. 18264096 2008
dbSNP: rs4811196
rs4811196
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0177804
Disease:
Bone Mineral Density Test
0.700 GeneticVariation GWASDB Genome-wide association with bone mass and geometry in the Framingham Heart Study. 17903296 2007
dbSNP: rs4811196
rs4811196
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0005938
Disease:
Bone Density
0.700 GeneticVariation GWASCAT Genome-wide association with bone mass and geometry in the Framingham Heart Study. 17903296 2007
dbSNP: rs6013029
rs6013029
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0028754
Disease:
Obesity
0.020 GeneticVariation BEFREE However, in meta-analyses of the present and the previous study, both the rs6013029 T-allele and the rs6020846 G-allele increased the risk of developing morbid obesity (rs6013029: OR(combined) = 1.36 [1.12-1.64], p = 0.002; rs6020846: OR(combined) = 1.26 [1.06-1.51], p = 0.01), and obesity (rs6013029</span>: OR(combined) = 1.17 [1.04-1.31], p = 0.007; rs6020846: OR(combined) = 1.17 [1.05-1.30], p = 0.004). 19245693 2009
dbSNP: rs6013029
rs6013029
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0028754
Disease:
Obesity
0.020 GeneticVariation BEFREE Those subjects who were homozygous for the rs6013029 T allele had 1.42-fold increased odds of obesity compared with those without the T allele. 18325910 2008
dbSNP: rs1368214237
rs1368214237
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis
0.010 GeneticVariation BEFREE Here, D-NAP was tested as prophylactic as well as therapeutic treatment for amytrophic lateral sclerosis (ALS) in the widely used TgN(SOD1-G93A)1Gur transgenic mouse model. 22956189 2012
dbSNP: rs6013029
rs6013029
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0028756
Disease:
Obesity, Morbid
0.010 GeneticVariation BEFREE However, in meta-analyses of the present and the previous study, both the rs6013029 T-allele and the rs6020846 G-allele increased the risk of developing morbid obesity (rs6013029: OR(combined) = 1.36 [1.12-1.64], p = 0.002; rs6020846: OR(combined) = 1.26 [1.06-1.51], p = 0.01), and obesity (rs6013029: OR(combined) = 1.17 [1.04-1.31], p = 0.007; rs6020846: OR(combined) = 1.17 [1.05-1.30], p = 0.004). 19245693 2009
dbSNP: rs6020846
rs6020846
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE However, in meta-analyses of the present and the previous study, both the rs6013029 T-allele and the rs6020846 G-allele increased the risk of developing morbid obesity (rs6013029: OR(combined) = 1.36 [1.12-1.64], p = 0.002; rs6020846: OR(combined) = 1.26 [1.06-1.51], p = 0.01), and obesity (rs6013029: OR(combined) = 1.17 [1.04-1.31], p = 0.007; rs6020846: OR(combined) = 1.17 [1.05-1.30], p = 0.004). 19245693 2009
dbSNP: rs6020846
rs6020846
Entrez Id: 56259
Gene Symbol: CTNNBL1
CTNNBL1
CUI: C0028756
Disease:
Obesity, Morbid
0.010 GeneticVariation BEFREE However, in meta-analyses of the present and the previous study, both the rs6013029 T-allele and the rs6020846 G-allele increased the risk of developing morbid obesity (rs6013029: OR(combined) = 1.36 [1.12-1.64], p = 0.002; rs6020846: OR(combined) = 1.26 [1.06-1.51], p = 0.01), and obesity (rs6013029: OR(combined) = 1.17 [1.04-1.31], p = 0.007; rs6020846: OR(combined) = 1.17 [1.05-1.30], p = 0.004). 19245693 2009