rs6021191
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Acute lymphocytic leukemia
0.010
GeneticVariation
BEFREE
RNA-seq data available from 65 SJCRH ALL tumor samples and 52 Yoruba HapMap samples showed that samples carrying the rs6021191 variant had higher NFATC2 expression compared with noncarriers (P = 1.1 × 10(-3) and 0.03, respectively).
25987655
2015
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
rs6021191
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Adult Acute Lymphocytic Leukemia
0.010
GeneticVariation
BEFREE
RNA-seq data available from 65 SJCRH ALL tumor samples and 52 Yoruba HapMap samples showed that samples carrying the rs6021191 variant had higher NFATC2 expression compared with noncarriers (P = 1.1 × 10(-3) and 0.03, respectively).
25987655
2015
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
rs17728960
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
C
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs17801791
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
A
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
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
rs6021264
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
G
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs6021268
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
C
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs6096463
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
A
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs6123048
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
G
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
rs6126249
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Allergic Reaction
A
0.700
GeneticVariation
GWASDB
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
23817569
2013
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
rs6021268
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Blood basophil count (lab test)
C
0.700
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
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
rs6021247
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Cardiovascular Diseases
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs6021191
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Childhood Acute Lymphoblastic Leukemia
0.010
GeneticVariation
BEFREE
RNA-seq data available from 65 SJCRH ALL tumor samples and 52 Yoruba HapMap samples showed that samples carrying the rs6021191 variant had higher NFATC2 expression compared with noncarriers (P = 1.1 × 10(-3) and 0.03, respectively).
25987655
2015
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
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
rs12625547
×
Entrez Id:
4773
Gene Symbol:
NFATC2
NFATC2
Eczema
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
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
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
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