IL13, interleukin 13, 3596

N. diseases: 587; N. variants: 9
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: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C1869116
Disease: ASTHMA, SUSCEPTIBILITY TO (finding)
ASTHMA, SUSCEPTIBILITY TO (finding) 		0.700 0
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C4017540
Disease: ALLERGIC RHINITIS, SUSCEPTIBILITY TO
ALLERGIC RHINITIS, SUSCEPTIBILITY TO 		0.700 0
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.800 1.000 1 2012 2012
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.800 1.000 1 2013 2013
dbSNP: rs115008099
rs115008099 		1.000 0.080 5 132656189 intron variant C/T snv 0.15
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs115008099
rs115008099 		1.000 0.080 5 132656189 intron variant C/T snv 0.15
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs12188917
rs12188917 		1.000 0.120 5 132655393 intron variant T/C;G snv
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0013595
Disease: Eczema
Eczema 		Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1295686
rs1295686 		0.882 0.160 5 132660151 intron variant T/A;C snv 0.68
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs848
rs848 		0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		Immune System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs848
rs848 		0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		Skin and Connective Tissue Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1295685
rs1295685 		0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1295686
rs1295686 		0.882 0.160 5 132660151 intron variant T/A;C snv 0.68
CUI: C0024902
Disease: Mastodynia
Mastodynia 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2012 2012
dbSNP: rs1295686
rs1295686 		0.882 0.160 5 132660151 intron variant T/A;C snv 0.68
CUI: C0553713
Disease: BREAST PAIN FEMALE
BREAST PAIN FEMALE 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs1295686
rs1295686 		0.882 0.160 5 132660151 intron variant T/A;C snv 0.68
CUI: C4531177
Disease: Sleep onset Insomnia
Sleep onset Insomnia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1295686
rs1295686 		0.882 0.160 5 132660151 intron variant T/A;C snv 0.68
CUI: C4554344
Disease: IgE-mediated food allergy
IgE-mediated food allergy 		Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0018621
Disease: Hay fever
Hay fever 		Respiratory Tract Diseases; Immune System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0003615
Disease: Appendicitis
Appendicitis 		Digestive System Diseases; Infections 0.010 1.000 1 2020 2020
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0003864
Disease: Arthritis
Arthritis 		Musculoskeletal Diseases 0.010 1.000 1 2011 2011