×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Alcohol consumption
0.100
GeneticVariation
GWASCAT
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
30698716
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
28452372
2017
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
31451708
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
31152163
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
26831199
2016
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis.
31015462
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Leukemia, Myelocytic, Acute
0.100
GeneticVariation
GWASCAT
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
27903959
2017
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Creatinine measurement, serum (procedure)
0.100
GeneticVariation
GWASCAT
1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
28452372
2017
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Creatinine measurement, serum (procedure)
0.100
GeneticVariation
GWASCAT
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
26831199
2016
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Low density lipoprotein cholesterol measurement
0.100
GeneticVariation
GWASCAT
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
30275531
2018
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Triglycerides measurement
0.100
GeneticVariation
GWASCAT
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
30275531
2018
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Triglycerides measurement
0.100
GeneticVariation
GWASCAT
Exome-wide association study of plasma lipids in >300,000 individuals.
29083408
2017
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Triglycerides measurement
0.100
GeneticVariation
GWASCAT
Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions.
30698716
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Uric acid measurement (procedure)
0.100
GeneticVariation
GWASCAT
Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.
30993211
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Uric acid measurement (procedure)
0.100
GeneticVariation
GWASCAT
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels.
31578528
2019
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Uric acid measurement (procedure)
0.100
GeneticVariation
GWASCAT
Modulation of genetic associations with serum urate levels by body-mass-index in humans.
25811787
2015
×
Entrez Id:
29974
Gene Symbol:
A1CF
A1CF
Serum total cholesterol measurement
0.100
GeneticVariation
GWASCAT
Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.
30275531
2018
×
Entrez Id:
2
Gene Symbol:
A2M
A2M
Adolescent idiopathic scoliosis
0.100
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018
×
Entrez Id:
2
Gene Symbol:
A2M
A2M
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.100
GeneticVariation
GWASCAT
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
30019117
2018
×
Entrez Id:
127550
Gene Symbol:
A3GALT2
A3GALT2
Body mass index
0.100
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
×
Entrez Id:
53947
Gene Symbol:
A4GALT
A4GALT
Red Blood Cell Count measurement
0.100
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
×
Entrez Id:
53947
Gene Symbol:
A4GALT
A4GALT
Red Blood Cell Count measurement
0.100
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
×
Entrez Id:
53947
Gene Symbol:
A4GALT
A4GALT
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
A catalog of genetic loci associated with kidney function from analyses of a million individuals.
31152163
2019
×
Entrez Id:
53947
Gene Symbol:
A4GALT
A4GALT
Glomerular Filtration Rate
0.100
GeneticVariation
GWASCAT
Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
31451708
2019
×
Entrez Id:
53947
Gene Symbol:
A4GALT
A4GALT
Hematocrit procedure
0.100
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016