NFATC2, nuclear factor of activated T cells 2, 4773

N. diseases: 154; N. variants: 22
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6021270
rs6021270
20 51524725 intron variant T/C snv 5.7E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs6021247
rs6021247
1.000 0.080 20 51492442 intron variant G/A snv 0.65
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 3 2018 2019
dbSNP: rs12625547
rs12625547
0.925 0.080 20 51538108 intron variant T/G snv 0.18
CUI: C0042345
Disease: Varicosity
Varicosity
Cardiovascular Diseases 0.700 1.000 2 2018 2019
dbSNP: rs12625547
rs12625547
0.925 0.080 20 51538108 intron variant T/G snv 0.18
CUI: C0013595
Disease: Eczema
Eczema
Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs16996066
rs16996066
0.925 0.040 20 51519305 intron variant C/T snv 4.1E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs16996066
rs16996066
0.925 0.040 20 51519305 intron variant C/T snv 4.1E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs17728960
rs17728960
20 51513177 intron variant T/C snv 5.1E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs17801791
rs17801791
20 51522481 intron variant C/A;G snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs193091397
rs193091397
1.000 0.040 20 51467037 intron variant A/G snv 1.2E-03
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs3787184
rs3787184
1.000 0.120 20 51541298 intron variant A/G snv 0.17
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs3787184
rs3787184
1.000 0.120 20 51541298 intron variant A/G snv 0.17
CUI: C2607914
Disease: Allergic rhinitis (disorder)
Allergic rhinitis (disorder)
Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3787186
rs3787186
20 51536805 intron variant T/C snv 0.68
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs4396773
rs4396773
1.000 0.040 20 51392255 intron variant C/T snv 0.43
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6013210
rs6013210
1.000 0.040 20 51549095 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.700 1.000 1 2011 2011
dbSNP: rs6013210
rs6013210
1.000 0.040 20 51549095 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs6021191
rs6021191
0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02
Precursor Cell Lymphoblastic Leukemia Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs6021247
rs6021247
1.000 0.080 20 51492442 intron variant G/A snv 0.65
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs6021247
rs6021247
1.000 0.080 20 51492442 intron variant G/A snv 0.65
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs6021247
rs6021247
1.000 0.080 20 51492442 intron variant G/A snv 0.65
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6021247
rs6021247
1.000 0.080 20 51492442 intron variant G/A snv 0.65
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2018 2018
dbSNP: rs6021264
rs6021264
20 51518144 intron variant A/G snv 6.1E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs6021268
rs6021268
20 51524602 intron variant T/C snv 5.8E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs6021268
rs6021268
20 51524602 intron variant T/C snv 5.8E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs6021268
rs6021268
20 51524602 intron variant T/C snv 5.8E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs6021276
rs6021276
1.000 0.080 20 51538847 intron variant T/C snv 0.70
Diabetes Mellitus, Non-Insulin-Dependent
Nutritional and Metabolic Diseases; Endocrine System Diseases 0.700 1.000 1 2019 2019