Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1818782
rs1818782
C9 ; DAB2
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs2489201
rs2489201
CACNB2
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs139761834
rs139761834
CD36
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs596406
rs596406
CELF2
G 0.700 GeneticVariation GWASCAT Genome-wide association study of liver enzymes in korean children. 24124411

2013
dbSNP: rs892295
rs892295
CHL1
A 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661

2012
dbSNP: rs10509735
rs10509735
CNNM1
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs333947
rs333947
CSF1
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs79105258
rs79105258
CUX2
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs10165093
rs10165093
EFHD1
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs34010237
rs34010237
FCGRT
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs76850691
rs76850691
GOT1
C 0.700 GeneticVariation GWASCAT The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. 30718733

2019
dbSNP: rs76850691
rs76850691
GOT1
C 0.700 GeneticVariation GWASCAT Genome-wide association study of liver enzymes in korean children. 24124411

2013
dbSNP: rs73550818
rs73550818
GOT2
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs9389268
rs9389268
HBS1L
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs11066280
rs11066280
HECTD4
0.700 GeneticVariation GWASCAT The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. 30718733

2019
dbSNP: rs72838936
rs72838936
HPSE2
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010

2018
dbSNP: rs147627531
rs147627531
KCNIP4
0.700 GeneticVariation GWASCAT Biomarker and Genomic Risk Factors for Liver Function Test Abnormality in Hazardous Drinkers. 30589442

2019
dbSNP: rs6455128
rs6455128
KHDRBS2
0.700 GeneticVariation GWASCAT A genome-wide association study identifies protein quantitative trait loci (pQTLs). 18464913

2008
dbSNP: rs862946
rs862946
LINC02306
A 0.700 GeneticVariation GWASCAT Genome-wide association study of liver enzymes in korean children. 24124411

2013
dbSNP: rs77213573
rs77213573
LINC02608
0.700 GeneticVariation GWASCAT Biomarker and Genomic Risk Factors for Liver Function Test Abnormality in Hazardous Drinkers. 30589442

2019
dbSNP: rs73154660
rs73154660
LOC101928236
0.700 GeneticVariation GWASCAT Biomarker and Genomic Risk Factors for Liver Function Test Abnormality in Hazardous Drinkers. 30589442

2019
dbSNP: rs17109512
rs17109512
LOC105378449
0.800 GeneticVariation GWASDB We carried out a genome-wide association study of serum aspartate aminotransferase (AST) activity in 866 Amish participants of the Heredity and Phenotype Intervention Heart Study and identified significant association of AST activity with a cluster of single nucleotide polymorphisms located on chromosome 10q24.1 (peak association was rs17109512; P=2.80E-14), in the vicinity of GOT1, the gene encoding cytosolic AST (cAST). 21900944

2011
dbSNP: rs17109512
rs17109512
LOC105378449
0.800 GeneticVariation GWASCAT We carried out a genome-wide association study of serum aspartate aminotransferase (AST) activity in 866 Amish participants of the Heredity and Phenotype Intervention Heart Study and identified significant association of AST activity with a cluster of single nucleotide polymorphisms located on chromosome 10q24.1 (peak association was rs17109512; P=2.80E-14), in the vicinity of GOT1, the gene encoding cytosolic AST (cAST). 21900944

2011
dbSNP: rs2477664
rs2477664
MRC1
T 0.700 GeneticVariation GWASCAT Genome-wide association study of hematological and biochemical traits in a Japanese population. 20139978

2010
dbSNP: rs2078087
rs2078087
NMNAT2
A 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661

2012