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: 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: rs6096463
rs6096463
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
dbSNP: rs6126249
rs6126249
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
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: 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: rs17728960
rs17728960
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
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
dbSNP: rs6021268
rs6021268
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C0200641
Disease:
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
dbSNP: rs6021268
rs6021268
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
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: C0042345
Disease:
Varicosity 		G 0.700 GeneticVariation GWASCAT Clinical and Genetic Determinants of Varicose Veins. 30566020 2018
dbSNP: rs6021264
rs6021264
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
dbSNP: rs6123048
rs6123048
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1527304
Disease:
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
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: 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: rs6021191
rs6021191
Entrez Id: 4773
Gene Symbol: NFATC2
NFATC2
CUI: C1961102
Disease:
Precursor Cell Lymphoblastic Leukemia Lymphoma 		T 0.700 GeneticVariation GWASCAT Genome-wide analysis links NFATC2 with asparaginase hypersensitivity. 25987655 2015
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: 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