Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1000005
rs1000005
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

dbSNP: rs10000770
rs10000770
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017

dbSNP: rs1000096
rs1000096
CUI: C1305855
Disease: Body mass index
Body mass index
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722

2019

dbSNP: rs10001414
rs10001414
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017

dbSNP: rs10001545
rs10001545
Alanine aminotransferase measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs10001545
rs10001545
Aspartate aminotransferase measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs10001545
rs10001545
Serum Alanine Aminotransferase Measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018

dbSNP: rs10002082
rs10002082
CUI: C0018810
Disease: heart rate
heart rate
A 0.700 GeneticVariation GWASCAT Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers. 29478026

2018

dbSNP: rs10002111
rs10002111
CUI: C1305855
Disease: Body mass index
Body mass index
A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722

2019

dbSNP: rs10002854
rs10002854
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017

dbSNP: rs10004892
rs10004892
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017

dbSNP: rs10005067
rs10005067
CUI: C0005938
Disease: Bone Density
Bone Density
T 0.700 GeneticVariation GWASCAT Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. 29304378

2018

dbSNP: rs10005233
rs10005233
CUI: C0003467
Disease: Anxiety
Anxiety
C 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. 29942085

2018

dbSNP: rs10005540
rs10005540
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

dbSNP: rs1000579
rs1000579
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
G 0.700 GeneticVariation GWASCAT Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. 28714907

2017

dbSNP: rs1000579
rs1000579
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
G 0.700 GeneticVariation GWASCAT Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. 28714907

2017

dbSNP: rs1000579
rs1000579
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders
0.700 GeneticVariation GWASCAT Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. 22004471

2012

dbSNP: rs1000579
rs1000579
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders
0.700 GeneticVariation GWASCAT Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. 22004471

2012

dbSNP: rs1000597
rs1000597
CUI: C0156257
Disease: Calculus of kidney and ureter
Calculus of kidney and ureter
0.700 GeneticVariation GWASCAT A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1. 22396660

2012

dbSNP: rs10006108
rs10006108
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017

dbSNP: rs10006235
rs10006235
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203

2019

dbSNP: rs10006235
rs10006235
CUI: C0021704
Disease: Intelligence
Intelligence
0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203

2019

dbSNP: rs10006237
rs10006237
CUI: C0596887
Disease: mathematical ability
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018

dbSNP: rs10006327
rs10006327
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
C 0.700 GeneticVariation GWASCAT Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. 30061737

2018

dbSNP: rs10006418
rs10006418
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959

2017