rs6021270
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
C
0.800
GeneticVariation
GWASCAT
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs6021270
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
C
0.800
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs12625547
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Varicosity
G
0.700
GeneticVariation
GWASCAT
Varicose veins of lower extremities: Insights from the first large-scale genetic study.
30998689
2019
rs12625547
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Eczema
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs3787186
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Red Blood Cell Count measurement
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs6013210
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Eosinophil count procedure
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Systolic Pressure
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Cardiovascular Diseases
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs6021276
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Diabetes Mellitus, Non-Insulin-Dependent
T
0.700
GeneticVariation
GWASCAT
Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population.
30718926
2019
rs12625547
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Varicosity
G
0.700
GeneticVariation
GWASCAT
Clinical and Genetic Determinants of Varicose Veins.
30566020
2018
rs16996066
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700
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
rs16996066
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Adolescent idiopathic scoliosis
0.700
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
rs3787184
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic rhinitis (disorder)
A
0.700
GeneticVariation
GWASCAT
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis.
30013184
2018
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Diastolic blood pressure
A
0.700
GeneticVariation
GWASCAT
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
30487518
2018
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Systolic Pressure
A
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Mean blood pressure
A
0.700
GeneticVariation
GWASCAT
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
30487518
2018
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Hypertensive disease
A
0.700
GeneticVariation
GWASCAT
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
30487518
2018
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Systolic Pressure
A
0.700
GeneticVariation
GWASCAT
Interethnic analyses of blood pressure loci in populations of East Asian and European descent.
30487518
2018
rs193091397
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Schizophrenia
0.700
GeneticVariation
GWASCAT
The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia.
28924203
2017
rs3787184
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
A
0.700
GeneticVariation
GWASCAT
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
29083406
2017
rs4396773
NFATC2;LOC105372663
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
rs754559199
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Body Height
T
0.700
GeneticVariation
GWASCAT
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.
28552196
2017
rs959996
NFATC2;LOC105372663
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
rs959996
NFATC2;LOC105372663
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
rs6021268
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
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