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: rs1881457
rs1881457 		0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457 		0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 < 0.001 1 2014 2014
dbSNP: rs1881457
rs1881457 		0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.010 < 0.001 1 2014 2014
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs1295686
rs1295686 		0.882 0.160 5 132660151 intron variant T/A;C snv 0.68
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.800 1.000 2 2013 2015
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: 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: 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: rs1881457
rs1881457 		0.790 0.280 5 132656717 intron variant A/C snv 0.21
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2013 2015
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: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2015 2015
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.010 < 0.001 1 2015 2015
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0014859
Disease: Esophageal Neoplasms
Esophageal Neoplasms 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0546837
Disease: Malignant neoplasm of esophagus
Malignant neoplasm of esophagus 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1800925
rs1800925 		0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs20541
rs20541 		0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs848
rs848 		0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2017 2017