rs1986734
|
|
Eosinophilic esophagitis
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
|
20208534 |
2010 |
rs9992101
|
|
Creatinine measurement, serum (procedure)
|
|
0.700 |
GeneticVariation
|
GWASCAT |
Genetic loci influencing kidney function and chronic kidney disease.
|
20383145 |
2010 |
rs17319721
|
|
Kidney Failure, Chronic
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
New loci associated with kidney function and chronic kidney disease.
|
20383146 |
2010 |
rs17319721
|
|
Creatinine measurement, serum (procedure)
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
New loci associated with kidney function and chronic kidney disease.
|
20383146 |
2010 |
rs13146355
|
|
Magnesium measurement
|
G |
0.800 |
GeneticVariation
|
GWASCAT |
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
|
20700443 |
2010 |
rs4859682
|
|
Glomerular Filtration Rate
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.
|
23535967 |
2013 |
rs10032549
|
|
Glomerular Filtration Rate
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.
|
23535967 |
2013 |
rs17319721
|
|
Glomerular Filtration Rate
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
|
26831199 |
2016 |
rs17319721
|
|
Creatinine measurement, serum (procedure)
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
|
26831199 |
2016 |
rs3923380
|
|
Goldenhar Syndrome
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia.
|
26853712 |
2016 |
rs1986734
|
|
Amino acids measurement
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.
|
27005778 |
2016 |
rs1986734
|
|
Protein measurement
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.
|
27005778 |
2016 |
rs5020545
|
|
Glomerular Filtration Rate
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.
|
27588450 |
2016 |
rs10008637
|
|
Hematocrit procedure
|
C |
0.700 |
GeneticVariation
|
GWASCAT |
Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.
|
27668658 |
2016 |
rs55940751
|
|
Systolic Pressure
|
C |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation.
|
27841878 |
2017 |
rs4859682
|
|
Red Blood Cell Count measurement
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
rs2870238
|
|
Hematocrit procedure
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
rs2870238
|
|
Hemoglobin measurement
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
rs6854652
|
|
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 |
rs6848817
|
|
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 |
rs6810716
|
|
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 |
rs4241595
|
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs13151434
|
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs13105942
|
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs10050141
|
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |