Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Vital capacity
CUI: C0042834
Disease: Vital capacity
0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
Vital capacity
CUI: C0042834
Disease: Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Carpal Tunnel Syndrome
CUI: C0007286
Disease: Carpal Tunnel Syndrome
0.700 GeneticVariation GWASCAT A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. 30833571 2019
Forced expiratory volume function
CUI: C0016529
Disease: Forced expiratory volume function
0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
Body Fat Distribution
CUI: C0424621
Disease: Body Fat Distribution
0.700 GeneticVariation GWASCAT Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. 30664634 2019
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
Smoking Behaviors
CUI: C1519383
Disease: Smoking Behaviors
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
Smoking
CUI: C0037369
Disease: Smoking
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
Physical Activity Measurement
CUI: C4049938
Disease: Physical Activity Measurement
0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936 2010
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. 20189936 2010
Height
CUI: C0489786
Disease: Height
0.700 GeneticVariation GWASDB Many sequence variants affecting diversity of adult human height. 18391951 2008
Body Height
CUI: C0005890
Disease: Body Height
0.700 GeneticVariation GWASCAT Many sequence variants affecting diversity of adult human height. 18391951 2008
Glioma
CUI: C0017638
Disease: Glioma
0.030 GeneticVariation BEFREE Moreover, the GG genotype of EFEMP1 rs3791679</span> was correlated with higher risk of glioma compared to the AA+GA genotype (OR = 2.60, 95%CI = 1.08-6.28) in the regressive model. 27706619 2016
Glioma
CUI: C0017638
Disease: Glioma
0.030 GeneticVariation BEFREE Moreover, we found that the GA+AA genotype of rs3791679 was associations with a heavy increased risk of glioma</span> in patients who have family history of cancers, and the OR (95% CI) was 6.81 (1.17-48.06). 26823870 2015
Glioma
CUI: C0017638
Disease: Glioma
0.030 GeneticVariation BEFREE Four SNPs were significant associated with glioma risk (rs1346787, P=0.004, adjusted OR=1.49; rs3791679, P=0.014, adjusted OR=1.27; rs1346786, P=0.002, adjusted OR=1.41; rs3791675, P=0.011, adjusted OR=1.27). 25638659 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
0.010 GeneticVariation BEFREE Moreover, we found that the GA+AA genotype of rs3791679 was associations with a heavy increased risk of glioma in patients who have family history of cancers, and the OR (95% CI) was 6.81 (1.17-48.06). 26823870 2015