IL2, interleukin 2, 3558

N. diseases: 950; N. variants: 5
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: rs2069772
rs2069772 		0.925 0.200 4 122451978 intron variant T/A;C snv
CUI: C0018621
Disease: Hay fever
Hay fever 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.800 1.000 1 2011 2011
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.710 1.000 2 2011 2013
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C1272321
Disease: Autoantibody measurement
Autoantibody measurement 		0.700 1.000 1 2011 2011
dbSNP: rs2069763
rs2069763 		0.807 0.320 4 122456327 synonymous variant C/A snv 0.36 0.29
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2069772
rs2069772 		0.925 0.200 4 122451978 intron variant T/A;C snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		Digestive System Diseases; Nutritional and Metabolic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2069772
rs2069772 		0.925 0.200 4 122451978 intron variant T/A;C snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C4721555
Disease: Autoimmune hepatitis
Autoimmune hepatitis 		Digestive System Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0271907
Disease: Acquired aplastic anemia
Acquired aplastic anemia 		Hemic and Lymphatic Diseases 0.010 < 0.001 1 2017 2017
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis 		Digestive System Diseases; Immune System Diseases 0.010 < 0.001 1 2018 2018
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2015 2015
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2010 2010
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0280856
Disease: Squamous cell carcinoma of vulva
Squamous cell carcinoma of vulva 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2008 2008
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.010 1.000 1 2020 2020
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0015230
Disease: Exanthema
Exanthema 		Skin and Connective Tissue Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		Infections; Respiratory Tract Diseases 0.010 1.000 1 2016 2016
dbSNP: rs2069762
rs2069762 		0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24
CUI: C0751606
Disease: Adult Acute Lymphocytic Leukemia
Adult Acute Lymphocytic Leukemia 		0.010 1.000 1 2018 2018