NFATC2, nuclear factor of activated T cells 2, 4773

N. diseases: 154; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6021270
rs6021270
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
dbSNP: rs6021270
rs6021270
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
dbSNP: rs12625547
rs12625547
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0042345
Disease:
Varicosity
G 0.700 GeneticVariation GWASCAT Varicose veins of lower extremities: Insights from the first large-scale genetic study. 30998689 2019
dbSNP: rs12625547
rs12625547
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0013595
Disease:
Eczema
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3787186
rs3787186
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6013210
rs6013210
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0007222
Disease:
Cardiovascular Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6021276
rs6021276
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0011860
Disease:
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
dbSNP: rs12625547
rs12625547
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0042345
Disease:
Varicosity
G 0.700 GeneticVariation GWASCAT Clinical and Genetic Determinants of Varicose Veins. 30566020 2018
dbSNP: rs16996066
rs16996066
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1837461
Disease:
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
dbSNP: rs16996066
rs16996066
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0410702
Disease:
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
dbSNP: rs3787184
rs3787184
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C2607914
Disease:
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
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0428883
Disease:
Diastolic blood pressure
A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0871470
Disease:
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
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0428886
Disease:
Mean blood pressure
A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0020538
Disease:
Hypertensive disease
A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs6021247
rs6021247
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0871470
Disease:
Systolic Pressure
A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs193091397
rs193091397
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. 28924203 2017
dbSNP: rs3787184
rs3787184
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
Allergic Reaction
A 0.700 GeneticVariation GWASCAT Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. 29083406 2017
dbSNP: rs4396773
rs4396773
Entrez Id: 4773;105372663
Gene Symbol: NFATC2;LOC105372663
NFATC2;LOC105372663
CUI: C0023467
Disease:
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
dbSNP: rs754559199
rs754559199
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0005890
Disease:
Body Height
T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs959996
rs959996
Entrez Id: 4773;105372663
Gene Symbol: NFATC2;LOC105372663
NFATC2;LOC105372663
CUI: C0023467
Disease:
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
dbSNP: rs959996
rs959996
Entrez Id: 4773;105372663
Gene Symbol: NFATC2;LOC105372663
NFATC2;LOC105372663
CUI: C0023467
Disease:
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
dbSNP: rs6021268
rs6021268
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0200638
Disease:
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