rs2072134
|
|
Alcohol consumption
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study.
|
28485404 |
2017 |
rs2072134
|
|
Alcohol consumption
|
A |
0.800 |
GeneticVariation
|
GWASCAT |
Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men.
|
21270382 |
2011 |
rs2072134
|
|
Alcohol consumption
|
A |
0.800 |
GeneticVariation
|
GWASDB |
Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men.
|
21270382 |
2011 |
rs2010549
|
|
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 |
rs2010604
|
|
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 |
rs2072134
|
|
High density lipoprotein measurement
|
A |
0.700 |
GeneticVariation
|
GWASCAT |
Protein and fat intake interacts with the haplotype of PTPN11_rs11066325, RPH3A_rs886477, and OAS3_rs2072134 to modulate serum HDL concentrations in middle-aged people.
|
31006500 |
2020 |
rs2072134
|
|
High density lipoprotein measurement
|
|
0.700 |
GeneticVariation
|
GWASCAT |
The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.
|
30718733 |
2019 |
rs2072135
|
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs2072135
|
|
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 |
rs2072136
|
|
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 |
rs2240187
|
|
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 |
rs2240188
|
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs2240189
|
|
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 |
rs2285932
|
|
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 |
rs4766678
|
|
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 |
rs6489882
|
|
Chronic Lymphocytic Leukemia
|
G |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia.
|
28165464 |
2017 |
rs6489882
|
|
Small Lymphocytic Lymphoma
|
G |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia.
|
28165464 |
2017 |
rs739903
|
|
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 |
rs757404
|
|
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 |
rs7961128
|
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation
|
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs2072136
|
|
Dengue Fever
|
|
0.020 |
GeneticVariation
|
BEFREE |
Polymorphisms in the OAS1 SNPs (rs1131454), OAS2 SNPs (rs1293762, rs15895 and rs1732778) and OAS3 SNPs (rs2285932 and rs2072136) genes were studied using PCR followed by restriction fragment length polymorphism methods in 30 patients for dengue infection and 40 control group who have no documented evidence of symptomatic dengue.
|
24819159 |
2015 |
rs2072136
|
|
Dengue Fever
|
|
0.020 |
GeneticVariation
|
BEFREE |
Polymorphisms in the OAS1 (rs1131454 and rs10774671), OAS3 (rs2285932 and rs2072136) and OAS2 (rs15895 and rs1732778) genes were studied using PCR followed by restriction fragment length polymorphism methods in 109 patients hospitalized for dengue (DEN) and 105 healthy controls (HCs) who have no documented evidence of symptomatic dengue.
|
23337612 |
2013 |
rs1859330
|
|
Enterovirus 71 infection
|
|
0.010 |
GeneticVariation
|
BEFREE |
Association of the OAS3 rs1859330 G/A genetic polymorphism with severity of enterovirus-71 infection in Chinese Han children.
|
28444539 |
2017 |
rs2072134
|
|
Hypertensive disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
Five gene variants, rs11066280 (C12orf51), rs12229654 and rs3782889 (MYL2), rs2072134 (OAS3), rs2093395 (TREML2), and rs17249754 (ATP2B1), were found to be associated with hypertension mostly in men (P = 4.76 × 10(-14) to 4.46 × 10(-7) in the joint analysis); three SNPs (rs11066280, rs12229654, and rs3782889) remained significant after Bonferroni correction in an independent population.
|
24142389 |
2014 |
rs2072135
|
|
Chronic Lymphocytic Leukemia
|
|
0.010 |
GeneticVariation
|
BEFREE |
While not attaining statistical significance (combined P-value = 1 × 10(-4)), rs2072135 defines a promising risk locus for CLL.
|
23668599 |
2013 |